What changed in this filing

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Item 2. Management’s Discussion and Analysis

2023-03-17 compared with 2022-09-14 · 139 added, 325 removed, 13 unchanged (97% of the section changed)

Discussion and Analysis of Financial Condition and Results of Operations.

stated otherwise, the words “we,” “us,” “our,” the “Company” or “Organicell”

in this Quarterly Report on Form 10-Q refer to Organicell Regenerative Medicine, Inc., a Nevada corporation, and its subsidiaries.

Note Regarding Forward- Looking Statements

statements contained in this Quarterly Report on Form 10-Q that are not historical facts are forward-looking statements within the meaning

of Section 27A of the Securities Act of 1933 (the “Securities Act”) and Section 21E of the Securities Exchange Act of 1934

(the “Exchange Act”).

These forward-looking statements are identified as any statement that does not relate strictly to historical

or current facts.

Statements using words such as “may,” “could,” “should,” “expect,”

“plan,” “project,” “strategy,” “forecast,” “intend,” “anticipate,”

“believe,” “estimate,” “predict,” “potential,” “pursue,” “target,”

“continue,” or similar expressions help identify forward-looking statements.

forward-looking statements contained in this Quarterly Report on Form 10-Q are largely based on our expectations, which reflect estimates

and assumptions made by our management.

These estimates and assumptions reflect our best judgment based on currently known market conditions

and other factors.

Although we believe such estimates and assumptions to be reasonable, they are inherently uncertain and involve a number

of risks and uncertainties that are beyond our control.

In addition, management’s assumptions about future events may prove to

be inaccurate.

Management cautions all readers that the forward-looking statements contained in this Quarterly Report on Form 10-Q are

not guarantees of future performance, and management cannot assure any reader that such statements will be realized or the forward-looking

events and circumstances will in fact occur.

The Company’s actual results may differ materially from those anticipated, estimated,

projected or expected by management.

forward-looking statements speak only as of the date of this Quarterly Report on Form 10-Q.

We do not intend to publicly update or revise

any forward-looking statements as a result of new information, future events or otherwise.

are a clinical-stage biopharmaceutical company principally focusing on the development of innovative biological therapeutics for the

treatment of degenerative diseases and the provision of other related services.

The Company’s proprietary products are derived

from perinatal sources and manufactured to retain the naturally occurring extracellular vesicles, hyaluronic acid, and proteins without

the addition or combination of any other substance or diluent (“RAAM Products”).

Our RAAM Products and related services are

principally used in the health care industry administered through doctors and clinics (“Providers”).

operates a placental tissue bank processing laboratory in Miami, Florida and Basalt, Colorado for the purpose of performing research

and development and the manufacturing and processing of the anti-aging and cellular therapy derived products that we sell and distribute

to our customers.

Company’s leading product, Zofin™ (also known as Organicell TM Flow), is an acellular, biologic therapeutic derived

from perinatal sources and is manufactured to retain naturally occurring microRNAs, without the addition or combination of any other

substance or diluent.

This product contains over 300 growth factors, cytokines, chemokines, and 102 unique microRNAs as well as other

extracellular vesicles/nanoparticles derived from perinatal tissues.

date, the Company has obtained certain Investigation New Drug (“IND”), and eighteen emergency IND (“eIND”) approvals

from the FDA, including applicable Institutional Review Board (“IRB”) approvals which authorized the Company to commence

clinical trials or treatments in connection with the use of Zofin™ and related treatment protocols.

The Company is pursuing efforts

to complete its already approved clinical studies (see below) as well as obtaining approval to commence additional studies for other

specific indications it has identified that the use of its products will provide more favorable and desired health related benefits for

patients seeking alternative treatment options than are currently available.

The ability of the Company to succeed in these efforts is

subject to among other things, the Company having sufficient available working capital to fund the substantial costs of completing clinical

trials, which the Company currently does not have, and ultimately, obtaining approval from the FDA.

FDA guidance which was announced in November 2017 and which became effective in May 2021 (postponed from November 2020 due to the COVID-19

pandemic) requires that the sale of products that fall under Section 351 of the Public Health Services Act pertaining to marketing traditional

biologics and human cells, tissues and cellular and tissue based products (“HCT/Ps”) can only be sold pursuant to an approved

biologics license application (“BLA”).

have not obtained any opinion or ruling regarding the Company’s operations and whether the processing, sales and distribution of

the products we currently produce would be subject to the FDA’s previously announced intended enforcement policies regarding HCT/P’s.

However, we do not believe that our products fall within these guidelines and intend to vigorously defend against any adverse interpretation

by the FDA on the classification of our products that may be deemed as falling under this defined regulation, if any.

Notwithstanding

the foregoing, we are undertaking efforts on an ongoing basis to mitigate any potential risks associated with an adverse ruling by the

FDA and the subsequent limitations on our ability to continue to generate revenues from the sale of our products in the United States

until the Company obtains the required licenses.

The efforts include continuing with clinical trials, expanding sales internationally

and developing new product offerings and/or designations of products that would not fall under these regulations.

June 2021, the Company announced that it was launching a service platform for its first autologous product called Patient Pure X TM

PPX TM is a non-manipulated biologic containing the nanoparticle fraction from a patient’s

own peripheral blood.

The Company began to accept minimal orders for this service since October 2021.

November 2020, the Company formed Livin’ Again Inc., a wholly owned subsidiary, for the purpose of among other things, providing

independent education, advertising and marketing services, to Providers that provide medical and other healthcare, anti-aging and regenerative

Due to limited activity to date, the Company intends to close-down this service by October 31, 2022.

impact on Economy and Business Environment

adverse public health developments and economic effects of the ongoing COVID-19 outbreak in the United States have adversely affected

the demand for our products and services by our customers and from patients of our customers as a result of quarantines, facility closures

and social distancing measures put into effect.

These restrictions have adversely affected the Company’s sales, results of operations

and financial condition.

Management’s Discussion and Analysis of Financial Condition and Results of Operations.

Unless stated otherwise, the words “we,” “us,” “our,” the “Company” or “Organicell” in this Quarterly Report on Form 10-Q refer to Organicell Regenerative Medicine, Inc., a Nevada corporation, and its subsidiaries.

Cautionary Note Regarding Forward- Looking Statements

The statements contained in this Quarterly Report on Form 10-Q that are not historical facts are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 (the “Securities Act”) and Section 21E of the Securities Exchange Act of 1934 (the “Exchange Act”).

These forward-looking statements are identified as any statement that does not relate strictly to historical or current facts.

Statements using words such as “may,” “could,” “should,” “expect,” “plan,” “project,” “strategy,” “forecast,” “intend,” “anticipate,” “believe,” “estimate,” “predict,” “potential,” “pursue,” “target,” “continue,” or similar expressions help identify forward-looking statements.

The forward-looking statements contained in this Quarterly Report on Form 10-Q are largely based on our expectations, which reflect estimates and assumptions made by our management.

These estimates and assumptions reflect our best judgment based on currently known market conditions and other factors.

Although we believe such estimates and assumptions to be reasonable, they are inherently uncertain and involve a number of risks and uncertainties that are beyond our control.

In addition, management’s assumptions about future events may prove to be inaccurate.

Management cautions all readers that the forward-looking statements contained in this Quarterly Report on Form 10-Q are not guarantees of future performance, and management cannot assure any reader that such statements will be realized or the forward-looking events and circumstances will in fact occur.

The Company’s actual results may differ materially from those anticipated, estimated, projected or expected by management.

All forward-looking statements speak only as of the date of this Quarterly Report on Form 10-Q.

We do not intend to publicly update or revise any forward-looking statements as a result of new information, future events or otherwise.

Business Overview

We are a clinical-stage biopharmaceutical company principally focusing on the development of innovative biological therapeutics for the treatment of degenerative diseases and regenerative medicine.

The Company’s proprietary products are derived from perinatal sources and manufactured to retain the naturally occurring extracellular vesicles, hyaluronic acid, and proteins without the addition or combination of any other substance or diluent (“RAAM Products”).

Our RAAM Products and related services are principally used in the health care industry administered through doctors and clinics (“Providers”).

Organicell operates an extracellular vesicle processing laboratory in Davie, Florida, and Basalt, Colorado each for the purpose of performing research and development and the manufacturing and processing of the anti-aging and cellular therapy derived products that we sell and distribute to our customers.

The Company’s leading product, Zofin™ (also known as Organicell™ Flow), is an acellular, biologic therapeutic derived from perinatal sources and is manufactured to retain naturally occurring microRNAs, without the addition or combination of any other substance or diluent.

This product contains over 300 growth factors, cytokines, chemokines, and 102 unique microRNAs as well as other exosomes/nanoparticles derived from perinatal tissues.

To date, the Company has obtained certain Investigational New Drug (“IND”), and 18 emergency IND (“eIND”) approvals from the FDA, including applicable Institutional Review Board (“IRB”) approvals which authorized the Company to commence clinical trials or treatments in connection with the use of Zofin™ and related treatment protocols.

The Company is pursuing efforts to complete its already approved clinical studies as well as obtaining approval to commence additional studies for other specific indications it has identified that the use of its products will provide more favorable and desired health related benefits for patients seeking alternative treatment options than are currently available.

The ability of the Company to succeed in these efforts is subject to among other things, the Company having sufficient available working capital to fund the substantial costs of completing clinical trials, which the Company currently does not have, and ultimately, obtaining approval from the FDA.

New FDA guidance which was announced in November 2017 and which became effective in May 2021 (postponed from November 2020 due to the COVID-19 pandemic) requires that the sale of products that fall under Section 351 of the Public Health Services Act pertaining to marketing traditional biologics and human cells, tissues and cellular and tissue based products (“HCT/Ps”) can only be sold pursuant to an approved biologics license application (“BLA”).

We have not obtained any opinion or ruling regarding the Company’s operations and whether the processing, sales and distribution of the products we currently produce would be subject to the FDA’s previously announced intended enforcement policies regarding HCT/P’s.

However, we do not believe that our products fall within these guidelines and intend to vigorously defend against any adverse interpretation by the FDA on the classification of our products that may be deemed as falling under this defined regulation, if any.

Notwithstanding the foregoing, we are undertaking efforts on an ongoing basis to mitigate any potential risks associated with an adverse ruling by the FDA and the subsequent limitations on our ability to continue to generate revenues from the sale of our products in the United States until the Company obtains the required licenses.

The efforts include continuing with clinical trials, expanding sales internationally and developing new product offerings and/or designations of products that would not fall under these regulations.

In June 2021, the Company announced that it was launching a service platform for its first autologous product called Patient Pure X TM (PPX TM ).

PPX TM is a non-manipulated biologic containing the nanoparticle fraction from a patient’s own peripheral blood.

The Company began to accept minimal orders for this service in October 2021 and to date revenues from PPX TM continue to be immaterial.

COVID-19 impact on Economy and Business Environment

The adverse public health developments and economic effects of the ongoing COVID-19 outbreak in the United States have adversely affected the demand for our products and services by our customers and from patients of our customers as a result of quarantines, facility closures and social distancing measures put into effect.

These restrictions have adversely affected the Company’s sales, results of operations and financial condition.

In response to the COVID-19 outbreak, the Company (a) has accelerated its research and development activities;

(b) has secured and is continuing to seek additional debt and/or equity financing to support working capital requirements;

and (c) continues

to take steps to stabilize and increase revenues from the sale of its products.

is no assurance as to when the adverse impact to the United States and worldwide economies resulting from the COVID-19 outbreak will

be eliminated, if at all, and whether any new or recurring pandemic outbreaks will occur again in the future causing a similar or worse

adverse impact on the United States and worldwide economies or our business.

following discussion of the Company’s results of operations and liquidity and capital resources should be read in conjunction with

our unaudited consolidated financial statements and related notes thereto appearing in Item 1 .

of this Quarterly Report on Form

of Operations

months ended July 31, 2022 as compared to three months ended July 31, 2021

Our revenues for the three months ended July 31, 2022 were $1,713,214, compared to revenues of $1,367,895 for the three months ended

July 31, 2021.

The increase in revenues during the three months ended July 31, 2022 of $345,319 or 25.2%, was primarily the result of

the Company being able to realize an increase of approximately 43.9% (approximately $601,300) in the average sales prices for the products

sold during the three months ended July 31, 2022 compared with the average sales prices realized on products sold during the three months

ended July 31, 2022, partially offset by a decrease of approximately 14.1% (approximately $276,800) in the overall unit sales of its

products during the three months ended July 31, 2022 compared with the three months ended July 31, 2021, and the Company’s ability

to generate approximately $20,800 of new revenues associated with its recently launched PPX TM service platform during the

three months ended July 31, 2022.

The increase in the average sales prices realized on products sold during the three months ended July

31, 2022 compared with the three months ended July 31, 2021, was due to increases in sales of higher priced medical grade product and

the reduction in volume pricing discounts granted to distributors for large orders of the Company’s medical grade product offerings,

partially offset from the reduction in the sales of the Company’s aesthetic product offerings, which are sold at lower prices than

the Company’s medical grade product offerings.

of Revenues .

Our cost of revenues for the three months ended July 31, 2022 were $208,749, compared with cost of revenues of $136,044

for the three months ended July 31, 2021.

The increase in the cost of revenues during the three months ended July 31, 2022 of $72,705

or 53.4%, compared with the three months ended July 31, 2021, was due to an increase in the cost of units sold of 78.5% (approximately

($106,800) during the three months ended July 31, 2022, compared to costs of units sold during the three months ended July 31, 2021,

partially offset from an decrease in the amount of units sold of 14.1% (approximately $34,100) during the three months ended July 31,

2022, compared with the three months ended July 31, 2021.

The increase in the cost of units sold was primarily the result of the Company’s

sales of higher cost medical grade product offerings, and the reduction of lower cost aesthetic product offerings.

Our gross profit for the three months ended July 31, 2022 was $1,504,465 (87.8% of revenues), compared with gross profit

of $1,231,851 (90.1% of revenues) for the three months ended July 31, 2021.

The increase in gross profit during the three months ended

July 31, 2022 of $272,614 was the result of the Company being able to realize an increases in the average sales prices for the products

sold during the three months ended July 31, 2022 and the new revenues associated with its recently launched PPX TM service

platform during the three months ended July 31, 2022, partially offset from increases in costs of units sold and decreases in the overall

unit sales of its products during the three months ended July 31, 2022 compared to the three months ended July 31, 2021.

and Administrative Expenses .

General and administrative expenses for the three months ended July 31, 2022 were $4,266,895, compared

with $2,624,808 for the three months ended July 31, 2021, an increase of $1,642,087 or 62.6%.

The increase in the general and administrative

expenses for the three months ended July 31, 2022 compared with the three months ended July 31, 2021, was primarily the result of an

increase in stock-based compensation costs to advisors, consultants and administrative staff totaling approximately $1,517,000, increases

in payroll and consulting fees of $148,000, increases in commissions due from sales of the Company’s products of approximately

$78,000, increased laboratory related costs of approximately $137,000 and the write-off of expired inventory associated with Livin Again

of $30,000, partially offset by decreased professional fees of approximately $69,000 and decreased research and development costs of

approximately $122,000.

The increase in stock-based compensation costs was principally the result of the shares issued as stock-based

compensation to the Company’s newly hired Chief Operating Officer and Acting Chief Executive Officer during the three months ended

July 31, 2022 compared with the three months ended 2021.

Income (Expense).

Other income for the three months ended July 31, 2022 was $34,973, compared with other (expense) of $15,951 for

the three months ended July 31, 2021.

The increase in other income of $50,924 during the three months ended July 31, 2022 compared to

the three months ended July 31, 2021, was principally the result of the gain from the write-off of liabilities attributable to discontinued

operations that had exceeded the “statute of limitations” of $125,851 and the decrease in the Commitment Fee Shortfall Obligation

of approximately $42,700 under our Securities Purchase Agreement with AJB (“SPA”) during the three months ended July 31,

2022 compared with the three months ended 2021, partially offset from increased costs of approximately $110,000 from the amortization

of discounts in connection with the $600,000 promissory note (“Note”) issued and sold by the Company to AJB Capital Investments,

LLC (“AJB”) in January 2022 and the increase of $16,000 in interest costs associated with the Note during the three months

ended July 31, 2022 compared with the three months ended July 31, 2021.

months ended July 31, 2022 as compared to nine months ended July 31, 2021

Our revenues for the nine months ended July 31, 2022 were $5,047,534, compared to revenues of $3,931,411 for the nine months ended July

The increase in revenues during the nine months ended July 31, 2022 of $1,116,123 or 28.3% was primarily the result of the

Company being able to realize an increase of approximately 33.0% (approximately $1,296,000) in the average sales prices for the products

sold during the nine months ended July 31, 2022 compared with the average sales prices realized on products sold during the nine months

ended July 31, 2021, partially offset by a decrease of approximately 5.3% (approximately $279,300) in the overall unit sales of its products

during the nine months ended July 31, 2022 compared with the nine months ended July 31, 2021, and the Company’s ability to generate

approximately $99,300 of new revenues associated with its recently launched PPX TM service platform during the nine months

ended July 31, 2022.

The increase in the average sales prices realized on products sold during the nine months ended July 31, 2022 compared

with the nine months ended July 31, 2021 was due to increases in sales of higher priced medical grade product and the reduction in volume

pricing discounts granted to distributors for large orders of the Company’s medical grade product offerings, partially offset from

the reduction in the sales of the Company’s aesthetic product offerings, which are sold at lower prices than the Company’s

medical grade product offerings.

of Revenues .

Our cost of revenues for the nine months ended July 31, 2022 were $484,287, compared with cost of revenues of $440,536

for the nine months ended July 31, 2021.

The increase in the cost of revenues during the nine months ended July 31, 2022 of $43,751 or

9.9% compared with the nine months ended July 31, 2021 was due to an increase in the cost of units sold of 16.1% (approximately ($71,100)

during the nine months ended July 31, 2022, compared to costs of units sold during the nine months ended July 31, 2021, partially offset

from an decrease in the amount of units sold of 5.3% (approximately $27,300) during the nine months ended July 31, 2022, compared with

the nine months ended July 31, 2021.

The increase in the cost of units sold was primarily the result of the Company’s sales of

higher cost medical grade product offerings, and the reduction of lower cost aesthetic product offerings.

Our gross profit for the nine months ended July 31, 2022 was $4,563,247 (90.4% of revenues), compared with gross profit of

$3,490,875 (88.8% of revenues) for the nine months ended July 31, 2021.

The increase in gross profit during the nine months ended July

31, 2022 of $1,072,372 was the result of the Company being able to realize an increases in the average sales prices for the products

sold during the nine months ended July 31, 2022 and the new revenues associated with its recently launched PPX TM service platform

during the nine months ended July 31, 2022, partially offset from increases in costs of units sold and decreases in the overall unit

sales of its products during the nine months ended July 31, 2022 compared to the nine months ended July 31, 2021.

and Administrative Expenses .

General and administrative expenses for the nine months ended July 31, 2022 were $10,225,371, compared

with $15,282,596 for the nine months ended July 31, 2021, a decrease of $5,057,225 or 33.1%.

The decrease in the general and administrative

expenses for the nine months ended July 31, 2022 compared with the nine months ended July 31, 2021, was primarily the result of a decrease

in stock-based compensation costs to advisors, consultants and administrative staff totaling approximately $5,535,400, reduced research

and development costs of approximately $465,000, partially offset by increases in payroll and consulting fees of $123,200, increases

in commissions due from sales of the Company’s products of approximately $417,900, increased professional fees of approximately

$151,400, increased laboratory and office related expenses of approximately $218,400 and the write-off of expired inventory associated

with Livin Again of $30,000.

The decrease in stock-based compensation costs was the result of a reduction in the amount of shares issued

as stock-based compensation during the nine months ended July 31, 2022 compared with the nine months ended July 31, 2021 and decreases

in the costs attributable to the shares issued as stock-based compensation based on decreases in the Company’s share price during

periods that the stock-based compensation was granted.

Income (Expense).

Other (expense) for the nine months ended July 31, 2022 was $215,112, compared with other (expense), net, of $6,687

for the nine months ended July 31, 2021.

The increase in other (expense), net, of $208,425 during the nine months ended July 31, 2022

compared to the nine months ended July 31, 2021 was principally the result of increased costs of approximately $272,000 from the amortization

of discounts in connection with the with the Note issued and sold by the Company to AJB in January 2022, the increase of $34,000 in interest

costs associated with the Note during the nine months ended July 31, 2022 compared with the nine months ended 2021, the increase in the

Commitment Fee Shortfall Obligation of approximately $17,700 under our SPA and the reduction in other income of approximately $25,100

from settlements received during the nine months ended July 31, 2022 compared with the nine months ended 2021, partially offset from

the gain from the write-off of liabilities attributable to discontinued operations that had exceeded the “statute of limitations”

of $125,851 during the nine months ended July 31, 2022 compared with the nine months ended July 31, 2021.

and Capital Resources

and Cash Equivalents

following table summarizes the sources and uses of cash for the periods stated.

The Company held no cash equivalents for any of the periods

Nine months Ended

and (c) continues to take steps to stabilize and increase revenues from the sale of its products.

There is no assurance as to when the adverse impact to the United States and worldwide economies resulting from the COVID-19 outbreak will be eliminated, if at all, and whether any new or recurring pandemic outbreaks will occur again in the future causing a similar or worse devastating impact to the United States and worldwide economies or our business.

The following discussion of the Company’s results of operations and liquidity and capital resources should be read in conjunction with our unaudited consolidated financial statements and related notes thereto appearing in Item 1 .

of this Quarterly Report on Form 10-Q.

Results of Operations

Three months ended January 31, 2023 as compared to three months ended January 31, 2022

Our revenues for the three months ended January 31, 2023 were $1,070,219, compared to revenues of $1,599,147 for the three months ended January 31, 2022.

The decrease in revenues during the three months ended January 31, 2023 of $528,928 or 33.1%, was primarily the result of a decrease of approximately 20.8% (approximately $274,500) in the overall unit sales of its products during the three months ended January 31, 2023 compared with the three months ended January 31, 2022, a decrease of approximately 15.0% (approximately $232,400) in the average sales prices for the products sold during the three months ended January 31, 2023 compared with the average sales prices realized on products sold during the three months ended January 31, 2023 and a decrease of approximately $22,000 of new revenues associated with its recently launched PPX TM service platform during the three months ended January 31, 2023 compared with the three months ended January 31, 2022.

The decrease in the average sales prices realized on products sold during the three months ended January 31, 2023 compared with the three months ended January 31, 2022, was due to decreases in sales of higher priced medical grade products, partially offset from the increase in the sales of the Company’s aesthetic product offerings, which are sold at lower prices than the Company’s medical grade product offerings.

Cost of Revenues .

Our cost of revenues for the three months ended January 31, 2023 were $104,313, compared with cost of revenues of $149,120 for the three months ended January 31, 2022.

The decrease in the cost of revenues during the three months ended January 31, 2023 of $44,807 or 30.1%, compared with the three months ended January 31, 2022, was due to a decrease in the amount of units sold of 20.1% (approximately $27,400) during the three months ended January 31, 2023, compared with the three months ended January 31, 2022 and a decrease in the cost of units sold of 11.7% (approximately ($17,400) during the three months ended January 31, 2023, compared to costs of units sold during the three months ended January 31, 2022.

The decrease in the cost of units sold was primarily the result of the Company’s decrease in sales of higher cost medical grade product offerings, partially offset from the increased in sales of lower cost aesthetic product offerings.

Gross Profit .

Our gross profit for the three months ended January 31, 2023 was $965,906 (90.3% of revenues), compared with gross profit of $1,450,027 (90.7% of revenues) for the three months ended January 31, 2022.

The decrease in gross profit during the three months ended January 31, 2023 of $484,121 was the result decreases in the average sales prices for the products sold during the three months ended January 31, 2023 and decreases in overall unit sales of its products during the three months ended January 31, 2023 compared to the three months ended January 31, 2022.

General and Administrative Expenses .

General and administrative expenses for the three months ended January 31, 2023 were $3,142,211, compared with $3,091,459 for the three months ended January 31, 2022, an increase of $50,752 or 1.6%.

The increase in the general and administrative expenses for the three months ended January 31, 2023 compared with the three months ended January 31, 2022, was primarily the result of an increase in stock-based compensation costs to advisors, consultants and administrative staff totaling approximately $446,200, increases in insurance costs of approximately $117,800, increased laboratory related costs of approximately $132,500 and increased investor relations costs of approximately $188,900, partially offset by decreased payroll and consulting fees of approximately $378,000, decreases in commissions from sales of the Company’s products and travel and entertainment costs of approximately $266,200, decreased professional fees of approximately $98,200 and decreased research and development costs of approximately $81,600.

The increase in stock-based compensation costs during the three months ended January 31, 2023 compared with the three months ended January 31, 2022 was principally the result of the amortization of costs from warrants issued as stock-based compensation to consultants in connection with the Restructuring in August 2022, stock issued as payment for services, and warrants issued to outside directors.

The increase in insurance costs during the three months ended January 31, 2023 compared with the three months ended January 31, 2022 was principally the result of the Company’s newly obtained directors & officers insurance policy in November 2023.

The decrease in payroll and consulting fees during the three months ended January 31, 2023 compared with the three months ended January 31, 2022 was principally the result of the Executives’ agreement to a reduction in salary and other compensation in connection with the Restructuring and reductions in fees paid to consultants.

The decreases in commissions on from sales of the Company’s products and travel and entertainment costs was principally the result of lower unit sales and overall revenues from the sale of the Company’s products during the three months ended January 31, 2023 compared with the three months ended January 31, 2022.

Other Expense.

Other expense for the three months ended January 31, 2023 was $110,351, compared with other expense of $52,304 for the three months ended January 31, 2022.

The increase in other expense of $58,047 during the three months ended January 31, 2023 compared to the three months ended January 31, 2022, was principally the result of the increase in the Commitment Fee Shortfall Obligation of approximately $37,400 under our Securities Purchase Agreement (“SPA 22”) with AJB Capital Investments, LLC (“AJB”) during the three months ended January 31, 2023 compared with the three months ended January 31, 2022 and increased interest costs of approximately $20,700 in connection with the $600,000 promissory note (“$600,000 Note”) issued and sold by the Company to AJB in January 2022 during the three months ended January 31, 2023 compared with the three months ended January 31, 2022.

Liquidity and Capital Resources

Cash and Cash Equivalents

The following table summarizes the sources and uses of cash for the periods stated.

The Company held no cash equivalents for any of the periods presented.

Three Months Ended

Cash, beginning of year

1 unchanged sentence

Net cash used in investing activities

Net cash provided by financing activities

Net cash (used in) provided by financing activities

Cash, end of period

the nine months July 31, 2022, the Company used cash in operating activities of $1,408,243, compared to $2,120,925 for the nine months

July 31, 2021, a decrease in cash used of $712,682.

The decrease in cash used in operating activities was due to the increase in revenues

and gross profit, the increase in accrued liabilities to management and the decrease in inventory balances during the nine months July

31, 2022 as compared to the nine months July 31, 2021, partially offset from the increase in cash to pay increasing operating expenses

on a current basis associated with professional fees, payroll, consulting costs and laboratory related expenses in connection with the

Company’s expansion of its research and development activities as well as payment of past due accounts payable and accrued expenses

during the nine months July 31, 2022 as compared to the nine months July 31, 2021.

the nine months July 31, 2022, the Company had cash used in investing activities of $516,519, compared to cash used in investing activities

of $224,809 for the nine months July 31, 2021.

The increase in cash used in investing activities of $291,710 was due primarily due payments

made in connection with the Company’s leasehold improvements associated with the new lab facility in Basalt, CO of approximately

$157,200 during the nine months July 31, 2022 as compared to the nine months July 31, 2021 and an increase in laboratory equipment purchased

for the Company’s laboratory facilities of approximately $134,500 during the nine months July 31, 2022 as compared to the nine

months July 31, 2021.

the nine months July 31, 2022, the Company had cash provided by financing activities of $1,890,857 compared to cash provided by financing

activities of $1,784,844 for the nine months July 31, 2021.

The increase in cash provided by financing activities of $106,013 was due

to increases in proceeds of $540,000 from the issuance of the Note to AJB, increases in capital contributed by executive of $250,000

and increases in advances for future stock purchases of $700,000 in connection with the Restructuring, partially offset from increases

in repayments of outstanding debt obligations of approximately $200,000 and the reduction in the sale of equity securities of approximately

$1,207,000 during the nine months July 31, 2022 as compared to the nine months July 31, 2021.

Company has historically relied on the sale of debt or equity securities, the restructuring of debt obligations and/or the issuance and/or

exchange of equity securities to meet the shortfall in cash to fund its operations.

During the nine months ended July 31, 2022 and through

the date of this report, the Company completed the following private sales of its securities:

November 2021, the Company sold an aggregate of 8,000,000 shares of common stock to one “accredited

investor” at $0.05 per share for an aggregate purchase price of $400,000.

were used for working capital.

January 2022, the Company sold an aggregate of 666,667 shares of common stock to one “accredited

investor” at $0.03 per share for an aggregate purchase price of $20,000.

price was paid through an offset of an outstanding balance owed by the Company to the investor

at the time of the sale of $20,000.

January 11, 2022, the Company entered into the SPA with AJB, pursuant to which we sold the

Note in the principal amount of $600,000 to AJB in a private transaction for a purchase price

of $540,000 (giving effect to original issue discount of $60,000).

The proceeds were used

for working capital.

February 2022, the Company sold an aggregate of 8,333,333 shares of common stock to one “accredited

investor” at $0.03 per share for an aggregate purchase price of $250,000.

were used for working capital.

August 2022, the Company sold an aggregate of 200,000,000 shares of common stock to four

“accredited investors” at $0.02 per share for an aggregate purchase price of

The proceeds are being used for working capital.

August 2022 and September 2022, the Company sold an aggregate of 62,500,000 shares of common

stock to three “accredited investors” at $0.04 per share for an aggregate purchase

price of $2,500,000.

The proceeds are being used for working capital.

Company issued the foregoing securities pursuant to the exemption from the registration requirements of the Securities Act afforded by

Section 4(a)(2) of the Securities Act and/or Regulation D promulgated thereunder.

Concern Consideration

unaudited accompanying consolidated financial statements have been prepared in conformity with generally accepted accounting principles,

which contemplate continuation of the Company as a going concern.

During the three months ended January 31, 2023, the Company used cash in operating activities of $1,282,724, compared to $559,994 for the three months ended January 31, 2022, an increase in cash used of $772,730.

The increase in cash used in operating activities was due to the decrease in revenues and gross profit, payment of past due accounts payable and accrued expenses, the decrease in accrued liabilities to management and the increase in inventory balances during the three months ended January 31, 2023 as compared to the three months ended January 31, 2022.

During the three months ended January 31,

2023, the Company had cash used in investing activities of $16,117, compared to cash used in investing activities of $155,134 for the

three months ended January 31, 2022, a decrease in cash used of $139,017.

The decrease in cash used in investing activities was primarily

due to the reduction in payments made for leasehold improvements associated with the new lab facility in Basalt, CO of approximately $102,000

and a decrease in laboratory equipment purchased for the Company’s laboratory facilities of approximately $37,000 during the three

months ended January 31, 2023 as compared to the three months ended January 31, 2022.

During the three months ended January 31,

2023, the Company had cash used in financing activities of $1,031,755 compared to cash provided by financing activities of $756,878 for

the three months ended January 31, 2022.

The decrease in cash provided by financing activities of $1,788,633 was due to decreases

in proceeds of $540,000 from the issuance of the $600,000 Note to AJB, increases in the escrow deposit for the share purchase of $500,000,

increases in repayment of notes payable of $429,000, increases in payments on finance leases of approximately $19,600 and the reduction

in the sale of equity securities of approximately $300,000 during the three months ended January 31, 2023 as compared to the three

months ended January 31, 2022.

Capital Resources

The Company has historically relied on the sale of debt or equity securities, the restructuring of debt obligations and/or the issuance and/or exchange of equity securities to meet the shortfall in cash to fund its operations.

Pursuant to the Purchase Agreement entered into with Tysadco Partners LLC, on December 2, 2022, the Company submitted a put request to Tysadco to purchase 4,456,326 registered shares at a purchase price (as calculated pursuant to the Purchase Agreement) of $0.02244, for a total of $100,000 (“Put Request”).

On December 5, 2022, Tysadco funded the Put Request and the Company issued 4,456,326 shares to Tysadco.

The proceeds from the share sale are being used for working capital and general corporate purposes.

On March 6, 2023, the Company entered into a

Securities Purchase Agreement (“SPA 23”) with AJB Capital, pursuant to which we sold a Promissory Note in the principal amount

of $530,000 (“$530,000 Note”) to AJB Capital in a private transaction to for a purchase price of $519,400 (giving effect to

original issue discount of $10,600).

In connection with the sale of the $530,000 Note, the Company also paid AJB Capital’s legal

fees and due diligence costs of $15,000, resulting in net proceeds to the Company of $504,400, which will be used for working capital

and other general corporate purposes.

Going Concern Consideration

The accompanying unaudited consolidated financial

statements have been prepared in conformity with generally accepted accounting principles, which contemplate continuation of the Company

as a going concern.

The Company has had limited revenues since its inception.

incurred net losses of $5,877,236 for the nine months ended July 31, 2022.

In addition, the Company had an accumulated deficit of $47,501,985

at July 31, 2022.

The Company had a negative working capital position of $6,451,479 at July 31, 2022.

United States Food and Drug Administration (“FDA”) regulations which were announced in November 2017 and which became effective

beginning in May 2021 (postponed from November 2020 due to the COVID-19 pandemic) require that the sale of products that fall under Section

351 of the Public Health Services Act pertaining to marketing traditional biologics and human cells, tissues and cellular and tissue

based products (“HCT/Ps”) can only be sold pursuant to an approved biologics license application (“BLA”).

Company has not obtained any opinion or ruling regarding the Company’s operations and whether the processing, sales and distribution

of the products it currently produces would be subject to the FDA’s previously announced intended enforcement policies regarding

addition to the above, the adverse public health developments and economic effects of the ongoing COVID-19 pandemic in the United States

have adversely affected the demand for our products and services by our customers and from patients of our customers as a result of quarantines,

facility closures and social distancing measures put into effect in connection with the COVID-19 outbreak and which currently still continue

to have a negative impact on our business and the economy in general.

a result of the above, the Company’s efforts to establish a stabilized source of sufficient revenues to cover operating costs has

yet to be achieved and ultimately may prove to be unsuccessful unless (a) the Company’s ability to process, sell and distribute

the products currently being produced or developed in the future are not restricted;

(b) the United States economy returns to pre-COVID-19

The Company incurred net losses of $2,286,656 for the three

months ended January 31, 2023.

In addition, the Company had an accumulated deficit of $52,807,962 at January 31, 2023.

had a working capital deficit of $773,385 at January 31, 2023.

United States Food and Drug Administration (“FDA”)

regulations which were announced in November 2017 and which became effective beginning in May 2021 (postponed from November 2020

due to the COVID-19 pandemic) require that the sale of products that fall under Section 351 of the Public Health Services Act pertaining

to marketing traditional biologics and human cells, tissues and cellular and tissue based products (“HCT/Ps”) can only be

sold pursuant to an approved biologics license application (“BLA”).

The Company has not obtained any opinion or ruling regarding

the Company’s operations and whether the processing, sales and distribution of the products it currently produces would be subject

to the FDA’s previously announced intended enforcement policies regarding HCT/P’s.

In addition to the above, the adverse public health developments associated with the ongoing COVID-19 pandemic combined with the downturn in the overall United States and global economies have adversely affected the demand for our products and services by our customers and from patients of our customers and which currently still continue to have a negative impact to our business and the economy.

As a result of the above, the Company’s efforts to establish a stabilized source of sufficient revenues to cover operating costs has yet to be achieved and ultimately may prove to be unsuccessful unless (a) the Company’s ability to process, sell and distribute the products currently being produced or developed in the future are not restricted;

(b) the United States economy returns to pre-COVID-19 conditions;

and/or (c) additional sources of working capital through operations or debt and/or equity financings are realized.

financial statements do not include any adjustments that might be necessary if the Company is unable to continue as a going concern.

anticipates that the Company will remain dependent, for the near future, on additional investment capital to fund ongoing operating expenses

and research and development costs related to development of new products and to perform required clinical studies in connection with

the sale of its products.

These financial statements do not include any adjustments that might be necessary if the Company is unable to continue as a going concern.

Management anticipates that the Company will remain dependent, for the near future, on additional investment capital to fund ongoing operating expenses and research and development costs related to development of new products and to perform required clinical studies in connection with the sale of its products.

The Company does not have any assets to pledge for the purpose of borrowing additional capital.

the Company relies on its ability to produce and sell products it manufactures that are subject to changing technology and regulations

that it currently sells and distributes to its customers.

The Company’s current market capitalization, common stock liquidity and

available authorized shares may hinder its ability to raise equity proceeds.

The Company anticipates that future sources of funding,

if any, will therefore be costly and dilutive, if available at all.

view of the matters described in the preceding paragraphs, recoverability of the recorded asset amounts shown in the accompanying consolidated

balance sheet assumes that (a) the Company is able to continue to produce products or obtain products under supply arrangements which

are in compliance with current and future regulatory guidelines;

In addition, the Company relies on its ability to produce and sell products it manufactures that are subject to changing technology and regulations that it currently sells and distributes to its customers.

The Company’s current market capitalization, common stock liquidity and available authorized shares may hinder its ability to raise equity proceeds.

The Company anticipates that future sources of funding, if any, will therefore be costly and dilutive, if available at all.

In view of the matters described in the preceding paragraphs, recoverability of the recorded asset amounts shown in the accompanying consolidated balance sheet assumes that (a) the Company is able to continue to produce products or obtain products under supply arrangements which are in compliance with current and future regulatory guidelines;

(b) the United States economy returns to pre-COVID-19 market conditions;

(c) the Company will be able to establish a stabilized source of revenues, including efforts to expand sales internationally and the

development of new product offerings and/or designations of products;

(c) the Company will be able to establish a stabilized source of revenues, including efforts to expand sales internationally and the development of new product offerings and/or designations of products;

(d) obligations to the Company’s creditors are not accelerated;

(e) the Company’s operating expenses remain at current levels and/or the Company is successful in restructuring and/or deferring

ongoing obligations;

(f) the Company is able to continue its research and development activities, particularly in regards to remaining

compliant with the FDA and ongoing safety and efficacy of its products;

and/or (g) the Company obtains additional working capital to

meet its contractual commitments and maintain the current level of Company operations through debt or equity sources.

is no assurance that the products we currently produce will not be subject to the FDA’s previously announced intended enforcement

policies regarding HCT/P’s and/or the Company will be able to complete its revenue growth strategy.

There is no assurance that

the Company’s research and development activities will be successful or that the Company will be able to timely fund the required

costs of those activities.

Without sufficient cash reserves, the Company’s ability to pursue growth objectives will be adversely

Furthermore, despite significant effort since July 2015, the Company has thus far been unsuccessful in achieving a stabilized

source of revenues.

revenues do not increase and stabilize, if the COVID-19 crisis is not satisfactorily managed and/or resolved, if the Company’s

ability to process, sell and/or distribute the products currently being produced or developed in the future are restricted, and/or

if additional funds cannot otherwise be raised, the Company might be required to seek other alternatives which could include the

sale of assets, closure of operations and/or protection under the U.S.

(e) the Company’s operating expenses remain at current levels and/or the Company is successful in restructuring and/or deferring ongoing obligations;

(f) the Company is able to continue its research and development activities, particularly in regards to remaining compliant with the FDA and ongoing safety and efficacy of its products;

and/or (g) the Company obtains additional working capital to meet its contractual commitments and maintain the current level of Company operations through debt or equity sources.

There is no assurance that the products we currently produce will not be subject to the FDA’s previously announced intended enforcement policies regarding HCT/P’s and/or the Company will be able to complete its revenue growth strategy.

There is no assurance that the Company’s research and development activities will be successful or that the Company will be able to timely fund the required costs of those activities.

Without sufficient cash reserves, the Company’s ability to pursue growth objectives will be adversely impacted.

Furthermore, despite significant effort since July 2015, the Company has thus far been unsuccessful in achieving a stabilized source of revenues.

If revenues do not increase and stabilize, if the Company’s ability to process, sell and/or distribute the products currently being produced or developed in the future are restricted, and/or if additional funds cannot otherwise be raised, the Company might be required to seek other alternatives which could include the sale of assets, closure of operations and/or protection under the U.S.

bankruptcy laws.

As of July 31, 2022, based on the

factors described above, the Company concluded that there was substantial doubt about its ability to continue to operate as a going

concern for the 12 months following the issuance of these financial statements.

Sheet Arrangements

liquidity is not dependent on the use of off-balance sheet financing arrangements (as that term is defined in Item 303(a) (4) (ii) of

Regulation S-K) and as of July 31, 2022 and through the date of this report, we had no such arrangements.

Issued Financial Accounting Standards

were no recently issued financial accounting standards that would have an impact on the Company’s financial statements.

Accounting Policies

unaudited consolidated financial statements reflect the selection and application of accounting policies which require us to make significant

estimates and judgments.

See Note 2 to our audited consolidated financial statements included in our Annual Report on Form 10-K for the

fiscal year ended October 31, 2021, “Summary of Significant Accounting Policies”.

As of January 31, 2023, based on the factors described above, the Company concluded that there was substantial doubt about its ability to continue to operate as a going concern for the 12 months following the issuance of these financial statements.

Off-Balance Sheet Arrangements

Our liquidity is not dependent on the use of off-balance sheet financing arrangements (as that term is defined in Item 303(a) (4) (ii) of Regulation S-K) and as of January 31, 2023 and through the date of this report, we had no such arrangements.

Recently Issued Financial Accounting Standards

There were no recently issued financial accounting standards that would have an impact on the Company’s financial statements.

Critical Accounting Policies

Our unaudited consolidated financial statements reflect the selection and application of accounting policies which require us to make significant estimates and judgments.

See Note 2 to our audited consolidated financial statements included in our Annual Report on Form 10-K for the fiscal year ended October 31, 2022, “Summary of Significant Accounting Policies”.

Quantitative and Qualitative Disclosures About Market Risk.

Not applicable.

Compared sentence by sentence after normalising whitespace, quotation marks, case and digits, so re-formatting and restated figures do not read as changed language. Wording changes appear as one removal and one addition. The current filing and the prior one are authoritative.

What changed 10-Q

Item 2. Management’s Discussion and Analysis