BioLife Solutions Announces 2012 Third Quarter Results: Ninth Straight Quarter of Record Revenue
135% Year-over-Year Growth in Third Quarter Revenues; 2012 Full Year Revenue Guidance Increased to $5.0 Million
PR Newswire
BOTHELL, Wash.

BOTHELL, Wash., Nov. 13, 2012 /PRNewswire/ -- BioLife Solutions, Inc. (OTCBB: BLFS), a leading developer, manufacturer and marketer of proprietary clinical grade hypothermic storage and cryopreservation freeze media for cells and tissues, and contract aseptic media manufacturer, today announced record revenue for the third quarter ended September 30, 2012.

(Logo: http://photos.prnewswire.com/prnh/20090814/BIOLIFELOGO)

Summary of Q3 2012 Achievements

During the third quarter of 2012, the Company accomplished the following:

  • Revenue of $1.7 million, BioLife's ninth sequential record revenue quarter.
  • No funds were required from investors in the quarter for the first time since the Company started operations.
  • Executed a new private-label distribution agreement to supply HypoThermosol® and CryoStor® to a leading life sciences cell culture tools provider.
  • Completed the build-out of its second Good Manufacturing Practice (cGMP) clean room suite.

Mike Rice, Chief Executive Officer, said, "This was another solid quarter for BioLife, as revenue ramped and we made strong progress in all operational areas of the Company.  Our presence in the high growth regenerative medicine field continues to expand, with several new accounts adopting HypoThermosol and CryoStor for use in their cellular and tissue therapies.  Our contract manufacturing team also reached a significant milestone with over $1.0 million in product shipments to our strategic customers. With our recent investments to expand our manufacturing capacity, we are well positioned to support the immense future growth of the tissue engineering and cellular therapy field while providing a best-in-class, trusted supply chain that is considered so critical to the clinical programs of our customers."

Third Quarter 2012 Financial Results

Total revenue for the third quarter of 2012 was $1.7 million, compared to $0.7 million in the same period of 2011. The increase of 135% from 2011 to 2012 was due primarily to contract manufacturing revenue and higher sales to customers in the cell and tissue banking and regenerative medicine market segments.

Gross margin in the quarter was 35.4% compared to 51.7% in the same quarter last year. The reduction in gross margin was attributable to higher cost of sales on contract manufacturing revenue and higher personnel and other costs included in cost of goods sold related to the expansion of the Company's facilities and production capacity.

Operating expenses in the third quarter were $744,000 compared with $655,000 in the third quarter of 2011 primarily attributable to increases related to strategic hires in all departments, partially offset by lower legal costs.

Other income/expense is primarily related to interest expense on the Company's notes payable.

For the third quarter, the Company reported a net loss of $352,000, or $(0.01) per share, a significant improvement over the third quarter of 2011 net loss of $479,000, or $(0.01) per share. Loss from operations in the quarter also improved to $149,000, compared to the $285,000 loss from operations in the third quarter of 2011.

Outlook for 2012

Management is increasing its revenue guidance to $5.0 million for the full year 2012, based on the expectation of higher sales to its contract-manufacturing customers. The Company also expects steady increases in revenue from existing and new customers in the regenerative medicine market segment, as well as continued growth through the Company's distribution network.

The Company expects gross margin to improve in the fourth quarter of 2012, however, to lower levels than the same period last year due to a higher mix of contract manufacturing revenue. Management expects operating expenses in the fourth quarter to remain at approximately the same level as the third quarter. 

Finally, management continues to believe the Company will achieve positive cash flow from operations in the fourth quarter of 2012.

About BioLife Solutions

BioLife Solutions develops, manufactures and markets patented hypothermic storage and cryopreservation solutions for cells and tissues.  The Company's proprietary HypoThermosol® and CryoStor® platform of solutions are marketed to academic and commercial organizations involved in cell therapy, tissue engineering, cord blood banking, drug discovery, and toxicology testing. BioLife's products are serum-free and protein-free, fully defined, and are formulated to reduce preservation-induced, delayed-onset cell damage and death.  BioLife's enabling technology provides academic and clinical researchers significant improvements in post-thaw cell, tissue, and organ viability and function.  For more information please visit www.biolifesolutions.com, and follow BioLife on Twitter.

This news release contains forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995.  These forward-looking statements include any statements that relate to the intent, belief, plans or expectations of the Company or its management, or that are not a statement of historical fact.  Any forward-looking statements in this news release are based on current expectations and beliefs and are subject to numerous risks and uncertainties that could cause actual results to differ materially. Some of the specific factors that could cause BioLife Solutions' actual results to differ materially are discussed in the Company's recent filings with the Securities and Exchange Commission.  BioLife Solutions disclaims any obligation to update any forward-looking statements as a result of developments occurring after the date of this press release. 

Media Relations:

Investor Relations:


Len Hall

Matt Clawson


Allen & Caron Inc

Allen & Caron Inc


(949) 474-4300

(949) 474-4300


len@allencaron.com

matt@allencaron.com
























BioLife Solutions, Inc.


Statement of Operations



Three Months

Ended September 30,



Nine Months

Ended September 30,



2012


2011



2012



2011

Revenue













  Product sales

$

1,676,480


$

710,518


$

3,599,770


$

1,934,165


  Licensing revenue


5,000



5,000



15,000



15,000

Total revenue


1,681,480



715,518



3,614,770



1,949,165


Cost of product sales


1,086,031



345,556



2.073,909



1,003,071


Gross profit


595,449



369,962



1,540,861



946,094

Operating expenses













     Research and development


110,689



98,903



353,837



391,086


     Sales and marketing


145,735



55,443



379,774



197,883


     General and administrative


487,733



500,424



1,441,852



1,356,222

Total operating expenses


744,157



654,770



2,175,463



1,945,191














Operating loss


(148,708)



(284,808)



(634,602)



(999,097)















Other income (expenses)













       Other income


––



20



94,253



43


       Interest expense


(185,554)



(171,677)



(547,875)



(497,458)


       Gain (loss) on disposal of equipment


431



(1,896)



368



(1,896)


       Amortization of deferred financing costs


(18,397)



(20,307)



(60,142)



(47,061)


Total other income (expenses)


(203,520)



(193,860)



(513,396)



(546,372)


Net Loss

$

(352,228)


$

(478,668)


$

(1,147,998)


$

(1,545,469)


Basic and diluted net loss per common share

$

(0.01)


$

(0.01)


$

(0.02)


$

(0.02)













Basic and diluted weighted average common shares used to calculate net loss per common share


69,679,854



69,679,854



69,679,854



69,679,854




























  Selected Balance Sheet Data

September 30,


December 31,



2012


2011


Cash and cash equivalents


$

7,529



$

16,864


Accounts receivable



797,943




547,143


Inventories



849,211




505,956


Total current assets



1,777,597




1,160,407


Total current liabilities



1,468,094




579,248


Promissory notes payable, related parties



10,603,127




10,128,127


Accrued interest, related parties



2,573,836




2,025,961


Total liabilities



15,453,615




12,842,503


Total shareholders' equity (deficiency)



(12,035,782)




(11,180,486)











  Selected Cash Flow Data

Nine Months Ended September 30,



2012


2011


Cash provided by (used in) operating activities


$

686,128



$

(797,122)


Cash used in investing activities



(1,170,463)




(55,972)


Cash provided by financing activities



475,000




870,000


Net increase (decrease) in cash and equivalents



(9,335)




16,906


SOURCE BioLife Solutions, Inc.

We believe the promise of cell and gene therapies starts with the integrity of a single cell

Advancing the future of cell and gene therapy

The human body can heal itself. Cell and gene therapies are designed to augment the patient’s ability to fight disease but only if the living cells behind those therapies remain viable and functional throughout the production processes. At BioLife Solutions, our mission is to protect the integrity of cells and provide trusted tools, services, and expertise that can enable our customers to advance the development and delivery of cell and gene therapies. We believe the future of cell and gene therapies hinges on the integrity of every single cell and we are here to protect that promise.

We understand the technical demands of bioprocessing in this field, and our advanced biopreservation expertise, cell culture optimization products, innovative storage systems, and closed-system manufacturing solutions are designed to enhance process efficiency, maintain cellular viability, and ensure reproducibility at every stage. Whether scaling up from R&D, navigating clinical trials or optimizing cryopreservation protocols for commercial production, we provide the tools and experience to streamline your workflow and safeguard your therapies.

Work with experts who understand your biopreservation challenges

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Collaborative and comprehensive CDMO support

At BioLife Solutions, we partner with leading contract development and manufacturing organizations (CDMOs) to enhance their biopreservation and cell processing capabilities. By providing advanced tools, regulatory support, and process optimization strategies, we empower CDMOs to better serve therapy developers, ensuring quality, consistency, and scalability in cell therapy manufacturing.

Regulatory
readiness

Navigating the complex regulatory landscape of cell and gene therapy requires a proactive approach. BioLife Solutions offers experienced regulatory support to help prepare your biopreservation and cell processing methods to meet global standards. From IND and BLA submissions to compliance with GMP, FDA, and EMA guidelines, our solutions help streamline approval pathways.

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STORE

CellSeal®
CryoCase

Alleviate CGT container challenges like fracture risk, bag burping or high rates of particulates

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Data-driven
decision making

Stay ahead with our comprehensive Evidence Library, a curated collection of scientific publications, white papers, and case studies demonstrating the efficacy of BioLife Solutions’ technologies. Access peer-reviewed research, real-world application data, and expert insights to support your bioprocessing and regulatory strategies.

Insights

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April 18, 2025

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March 27, 2025

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February 19, 2025

How to prepare early for regulatory submissions from IND to BLA

Preserve, protect and expand cell performance

Mastering
Biopreservation

Ensure Regulatory Submission Readiness

Automate & Close
CGT Processes

Protect & Expand
Cell Performance