blfs_10q.htm


UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
 
———————
FORM 10-Q

(Mark One)
þ  QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended March 31, 2014
 
¨  TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE
ACT OF 1934
For the transition period from     to

Commission File Number 0-18170
 
———————
BioLife Solutions, Inc.
(Exact name of registrant as specified in its charter)
 
———————

DELAWARE
94-3076866
(State or other jurisdiction of incorporation or organization)
(IRS Employer Identification No.)

3303 MONTE VILLA PARKWAY, SUITE 310, BOTHELL, WASHINGTON, 98021
(Address of registrant’s principal executive offices, Zip Code)
 
(425) 402-1400
(Telephone number, including area code)

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.  Yes þ  No ¨
 
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate website, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (S232.405 of this chapter) during the preceding 12 months (or for such shorter period that the Registrant was required to submit and post said files).  Yes þ  No ¨
 
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer”, “accelerated filer”, and “smaller reporting company” in Rule 12b-2 of the Exchange Act.  Large accelerated filer ¨ Accelerated filer ¨ Non-accelerated filer ¨ Smaller reporting company þ
 
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act).  Yes ¨  No þ
 
As of April 30, 2014 12,007,461 shares of the registrant’s common stock were outstanding.
 


 
 
 
 
 
BIOLIFE SOLUTIONS, INC.

FORM 10-Q

FOR THE QUARTER ENDED MARCH 31, 2014

TABLE OF CONTENTS
 
    Page
     
PART I.  FINANCIAL INFORMATION
   
       
Item 1. Financial Statements   3
       
    Balance Sheets as of March 31, 2014 (unaudited) and December 31, 2013   3
         
   
Statements of Operations (unaudited) for the three month periods Ended March 31, 2014 and 2013
  4
         
   
Statements of Cash Flows (unaudited) for the three month periods Ended March 31, 2014 and 2013
  5
         
    Notes to Financial Statements (unaudited)   6
       
Item 2.  Management’s Discussion and Analysis of Financial Condition and Results of Operations   11
       
Item 3. Quantitative and Qualitative Disclosures about Market Risk   16
       
Item 4.  Controls and Procedures   16
       
PART II. OTHER INFORMATION
   
       
Item 5. Other Information    17
       
Item 6. Exhibits   17
       
    Signatures   18
         
    Index to Exhibits    19
 
 
2

 
 
PART I.  FINANCIAL INFORMATION
 
 Item 1.
Financial Statements

BIOLIFE SOLUTIONS, INC.
Balance Sheets
 (unaudited)

 
March 31,
 
December 31,
 
 
2014
 
2013
 
Assets
           
Current assets
           
Cash and cash equivalents
 
$
12,839,600
   
$
156,273
 
Accounts receivable, trade, net of allowance for doubtful accounts of $1,100 at March 31, 2014 and December 31, 2013
   
1,325,564
     
1,009,316
 
Inventories
   
297,105
     
420,924
 
Prepaid expenses and other current assets
   
202,784
     
291,745
 
Total current assets
   
14,665,053
     
1,878,258
 
                 
Property and equipment
               
Leasehold improvements
   
1,121,362
     
1,121,362
 
Furniture and computer equipment
   
309,626
     
300,581
 
Manufacturing and other equipment
   
773,990
     
764,258
 
Subtotal
   
2,204,978
     
2,186,201
 
Less: Accumulated depreciation
   
(924,663
)
   
(862,157
)
Net property and equipment
   
1,280,315
     
1,324,044
 
Long term deposits
   
36,166
     
36,166
 
Deferred financing costs, net
   
––
     
114,874
 
Total assets
 
$
15,981,534
   
$
3,353,342
 
                 
Liabilities and Shareholders’ Equity (Deficiency)
               
Current liabilities
               
Accounts payable
 
$
707,983
   
$
867,070
 
Accrued expenses and other current liabilities
   
30,044
     
146,626
 
Accrued compensation
   
208,127
     
503,194
 
Deferred rent
   
117,501
     
111,250
 
Total current liabilities
   
1,063,655
     
1,628,140
 
Long term liabilities
               
Promissory notes payable, related parties
   
––
     
10,603,127
 
Accrued interest, related parties
   
––
     
3,501,610
 
Deferred rent, long term
   
840,730
     
891,986
 
Total liabilities
   
1,904,385
     
16,624,863
 
                 
Commitments and Contingencies (Note 7)
               
                 
Shareholders' equity (deficiency)
               
Common stock, $0.001 par value; 150,000,000 shares authorized, 11,941,619 and 5,029,920  shares issued and outstanding at March 31, 2014 and December 31, 2013
   
11,941
     
5,030
 
Additional paid-in capital
   
71,519,816
     
43,618,686
 
Accumulated deficit
   
(57,454,608
)
   
(56,895,237
)
Total shareholders' equity (deficiency)
   
14,077,149
     
(13,271,521
)
Total liabilities and shareholders' equity (deficiency)
 
$
15,981,534
   
$
3,353,342
 

The accompanying Notes to Financial Statements are an integral part of these financial statements
 
 
3

 
 
BIOLIFE SOLUTIONS, INC.
Statements of Operations
(unaudited)

   
Three Month Period Ended March 31,
 
   
2014
   
2013
 
Revenue
           
Product sales
 
$
2,065,030
   
$
1,550,845
 
Licensing revenue
   
––
     
609,167
 
Total revenue
   
2,065,030
     
2,160,012
 
Cost of product sales
   
1,161,641
     
1,034,528
 
Gross profit
   
903,389
     
1,125,484
 
Operating expenses
               
Research and development
   
167,287
     
105,968
 
Sales and marketing
   
241,400
     
202,758
 
General and administrative
   
863,743
     
624,427
 
Total  operating expenses
   
1,272,430
     
933,153
 
                 
Operating income (loss)
   
(369,041
)
   
192,331
 
                 
Other income (expenses)
               
Interest expense
   
(177,308
)
   
(185,555
)
Amortization of deferred financing costs
   
(13,022
)
   
(13,952
)
Total other income (expenses)
   
(190,330
)
   
(199,507
)
                 
Net Loss
 
$
(559,371
)
 
$
(7,176
)
                 
Basic and diluted net loss per common share
 
$
(0.10
)
 
$
(0.00
)
                 
Basic and diluted weighted average common shares used to calculate net loss per common share
   
5,568,802
     
4,990,971
 

The accompanying Notes to Financial Statements are an integral part of these financial statements
 
 
4

 

BIOLIFE SOLUTIONS, INC.
Statements of Cash Flows
 
(unaudited)

   
Three Month Period Ended March 31,
 
   
2014
   
2013
 
Cash flows from operating activities
               
Net loss
 
$
(559,371
)
 
$
(7,176
)
Adjustments to reconcile net loss to net cash used in operating activities
               
Depreciation
   
62,506
     
58,697
 
Stock-based compensation expense
   
51,619
     
67,382
 
Stock to be issued for services
   
80,000
     
––
 
Amortization of deferred financing costs
   
13,022
     
13,952
 
Lease incentives received from landlord, net of amortization of deferred rent related to lease incentives
   
(39,778
   
(13,333
                 
Change in operating assets and liabilities
               
(Increase) Decrease in
               
Accounts receivable, trade
   
(316,248
   
(376,004
Inventories
   
123,819
     
(20,041
)
Prepaid expenses and other current assets
   
88,961
     
(27,070
Increase (Decrease) in
               
Accounts payable
   
(159,087
)
   
191,419
 
Accrued compensation and other current liabilities
   
(411,650
   
(63,278
Accrued interest, related parties
   
177,308
     
185,555
 
Deferred rent
   
(5,227
)
   
(27,412
)
Deferred revenue
   
––
     
(109,167
Net cash used in operating activities
   
(894,126
)
   
(126,476
)
                 
Cash flows from investing activities
               
Purchase of property and equipment
   
(18,777
)
   
(33,937
)
Net cash used in investing activities
   
(18,777
)
   
(33,937
)
                 
Cash flows from financing activities
               
Proceeds from sale of common stock, net of expenses
   
13,596,230
     
––
 
Proceeds from exercise of common stock options
   
––
     
25,458
 
Net cash provided by financing activities
   
13,596,230
     
25,458
 
                 
Net increase (decrease) in cash and cash equivalents
   
12,683,327
     
(134,955
                 
Cash and cash equivalents - beginning of period
   
156,273
     
196,478
 
                 
Cash and cash equivalents - end of period
 
$
12,839,600
   
$
61,523
 
                 
Non-cash financing activities
               
Conversion of notes payable and related party accrued interest to equity, net of unamortized deferred finance costs (See Note 1)
 
$
14,180,193
   
$
––
 
 
The accompanying Notes to Financial Statements are an integral part of these financial statements
 
 
5

 
 
BIOLIFE SOLUTIONS, INC.

Notes to Financial Statements
(unaudited)

1.
Organization and Significant Accounting Policies

Business
 
BioLife Solutions, Inc. ("BioLife,” “us,” “we,” “our,” or the “Company”) develops, manufactures and markets patented hypothermic storage and cryopreservation solutions for cells and tissues.  The Company’s proprietary HypoThermosol® FRS, CryoStor®, and generic BloodStor®, and SAVSU®’s biopreservation media products and precision thermal packaging products are marketed to the biobanking, drug discovery, and regenerative medicine markets, including hospital-based stem cell transplant centers, pharmaceutical companies, cord blood and adult stem cell banks, hair transplant centers, and suppliers of cells to the drug discovery, toxicology testing and diagnostic markets. 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.  Additionally, for our direct, distributor, and contract customers, we perform custom formulation, fill, and finish services.
 
Basis of Presentation

We have prepared the accompanying unaudited financial statements pursuant to the rules and regulations of the Securities and Exchange Commission (the “SEC”). Pursuant to these rules and regulations, we have condensed or omitted certain information and footnote disclosures we normally include in our annual financial statements prepared in accordance with accounting principles generally accepted in the United States of America (“GAAP”). In management’s opinion, we have made all adjustments (consisting only of normal, recurring adjustments) necessary to fairly present our financial position, results of operations and cash flows. Our interim period operating results do not necessarily indicate the results that may be expected for any other interim period or for the full year. These financial statements and accompanying notes should be read in conjunction with the financial statements and notes thereto in our Annual Report on Form 10-K for the year ended December 31, 2013 on file with the SEC.

There have been no material changes to our significant accounting policies as compared to the significant accounting policies described in the financial statements in our Annual Report on Form 10-K for the year ended December 31, 2013.

Recent Developments

Reverse Stock Split
 
On January 17, 2014, our Board of Directors approved an amendment to our certificate of incorporation to effect a reverse stock split by a ratio of 1 for 14, with no reduction in the number of shares of common stock that were previously authorized in our certificate of incorporation.  The reverse stock split was effective on January 29, 2014.  Unless otherwise noted, all share and per share data in these financial statements give effect to the 1-for-14 reverse stock split of our common stock.
 
Public Offering of Units
 
On March 25, 2014, we closed a registered public offering of 3,588,878 units for gross proceeds of $15,432,175. Each unit consisted of one share of the Company’s common stock and one warrant, each warrant exercisable for seven years to purchase one share of the Company’s common stock at an exercise price of $4.75. Net of placement agent fees of $1,211,734 and offering costs of $624,211, we received net proceeds of $13,596,230.  Of the gross proceeds, $9.1 million was allocated to common stock and $6.3 million was allocated to warrants, based on relative fair values.
 
Conversion of Notes and Interest to Equity
 
Pursuant to previously disclosed note conversion agreements with WAVI Holding AG and Taurus4757 GmbH (the “Note Holders”), concurrently with the closing of the Company’s public offering of units, the Company converted approximately $14.3 million of indebtedness, including accrued interest, to the Note Holders into equity, issuing to the Note Holders an aggregate of 3,321,405 units having terms substantially similar to the public offering units.  In connection with the note conversion, the Company’s $14.3 million indebtedness to the Note Holders under the terms of the Company’s previously disclosed facility agreements was extinguished, all remaining unamortized deferred finance costs were recorded to additional paid in capital, and the Note Holders agreed to release all security interests. Of the total conversion amount, $8.4 million was allocated to common stock and $5.8 million was allocated to warrants, based on relative fair values.
 
 
6

 

Listing of Common Stock on NASDAQ Capital Market
 
On March 26, 2014, our common stock was listed on the Nasdaq Capital Market under the symbol BLFS.
 
Concentrations of credit risk and business risk

In the three months ended March 31, 2014 and 2013, we derived approximately 45% and 50%, respectively, of our product revenue from our relationship with one contract manufacturing customer. All license revenue recognized in the three months ended March 31, 2013 was derived from one customer. No other customer accounted for more than 10% of revenue in the three months ended March 31, 2014 or 2013.

Revenue from customers located in foreign countries represented 9% of total revenue during the three months ended March 31, 2014 and 2013.

At March 31, 2014, our contract manufacturing customer accounted for 47% of gross accounts receivable. At December 31, 2013, three customers accounted for approximately 64% of total gross accounts receivable.

Recent Accounting Pronouncements

There have been no new accounting pronouncements during the three month period ended March 31, 2014, as compared to our Annual Report on Form 10-K for the year ended December 31, 2013, that are of significance, or potential significance, to us.
 
2.
Inventory

Inventory consists of the following at March 31, 2014 and December 31, 2013:
 
   
March 31,
2014
   
December 31,
2013
 
Raw materials
 
$
179,858
   
$
334,031
 
Work in progress
   
33,650
     
14,570
 
Finished goods
   
83,597
     
72,323
 
Total
 
$
297,105
   
$
420,924
 
 
3.
Deferred Rent

Deferred rent consists of the following at March 31, 2014 and December 31, 2013:

   
March 31,
2014
   
December 31,
2013
 
Landlord-funded leasehold improvements
 
$
1,034,311
   
$
1,047,026
 
Less accumulated amortization
   
(160,126
   
(133,063
Total
   
874,185
     
913,963
 
Straight line rent adjustment
   
84,046
     
89,273
 
Total deferred rent
 
$
958,231
   
$
1,003,236
 

During the three month periods ended March 31, 2014 and 2013, the Company recorded $27,063 and $22,272, respectively, in deferred rent amortization of these landlord funded leasehold improvements.

Straight line rent adjustment represents the difference between cash rent payments and the recognition of rent expense on a straight-line basis over the terms of the lease.

 
7

 
 
4.
Share-based Compensation

Stock Options

The following is a summary of stock option activity for the three month period ended March 31, 2014, and the status of stock options outstanding at March 31, 2014:
 
   
Three Month Period Ended
 
   
March 31, 2014
 
         
Wtd. Avg.
 
         
Exercise
 
   
Options
   
Price
 
Outstanding at beginning of year
   
1,417,309
   
$
1.36
 
Granted
   
––
     
––
 
Exercised
   
––
     
––
 
Forfeited
   
(46,844
)
   
1.39
 
Expired
   
––
     
––
 
Outstanding at March 31, 2014
   
1,370,465
   
$
1.36
 
                 
 Stock options exercisable at March 31, 2014
   
1,248,342
   
$
1.20
 
 
As of March 31, 2014, there was $3,314,296 of aggregate intrinsic value of outstanding stock options, including $3,114,674 of aggregate intrinsic value of exercisable stock options.  Intrinsic value is the total pretax intrinsic value for all “in-the-money” options (i.e., the difference between the Company’s closing stock price on the last trading day of the quarter and the exercise price, multiplied by the number of shares) that would have been received by the option holders had all option holders exercised their options on March 31, 2014.  This amount will change based on the fair market value of the Company’s stock.
 
We recorded stock compensation expense related to options of $51,619 in the three months ended March 31, 2014 and $67,382 for the three month periods ended March 31, 2013, as follows:

   
Three Month Period Ended
 
   
March 31,
 
   
2014
   
2013
 
Research and development costs
 
 $
       8,135
   
$
       6,954
 
Sales and marketing costs
   
2,723
     
630
 
General and administrative costs
   
26,165
     
47,936
 
Cost of product sales
   
14,596
     
11,862
 
Total
 
 $
51,619
   
$
67,382
 
 
Management applies an estimated forfeiture rate that is derived from historical employee termination data.  The estimated forfeiture rate applied for the three month periods ended March 31, 2014 and 2013 was approximately 7%.
 
As of March 31, 2014, we had approximately $243,765 of unrecognized compensation expense related to unvested stock options.  We expect to recognize this compensation expense over a weighted average period of approximately 1.7 years.
 
Restricted Stock

At March 31, 2014, there were no unvested restricted stock units outstanding.

 
8

 
 
5.
Warrants

The following is a summary of warrant activity for the three month period ended March 31, 2014, and the status of warrants outstanding at March 31, 2014:
 
   
Three Month Period Ended
 
   
March 31, 2014
 
         
Wtd. Avg.
 
         
Exercise
 
   
Warrants
   
Price
 
Outstanding at beginning of year
   
517,858
   
$
1.02
 
Granted
   
6,910,283
     
4.75
 
Exercised
   
––
     
––
 
Forfeited/Expired
   
––
     
––
 
Outstanding at March 31, 2014
   
7,428,141
   
$
4.49
 
 
At March 31, 2014, we had 7,428,141 warrants outstanding and exercisable with a weighted average exercise price of $4.49. The outstanding warrants have expiration dates between November 2014 and March 2021.
 
As discussed in Note 1, during the quarter ended March 31, 2014, we issued 3,588,878 warrants with an expiration date of March 25, 2021 in connection with the Company’s public offering of units on March 25, 2014.   Each whole warrant is exercisable for a period of seven years to acquire one share of common stock with an exercise price of $4.75 per share. In addition, we issued 3,321,405 warrants with an expiration date of March 25, 2021 in connection with the conversion of approximately $14.3 million of indebtedness to the Company’s existing Note Holders into equity on March 25, 2014. Each whole warrant is exercisable for a period of seven years to acquire one share of common stock with an exercise price of $4.75 per share. There were no warrants exercised, forfeited or expired in the three month period ended March 31, 2014.
 
Deferred Financing Costs
 
During the quarter ended June 30, 2012, the Company issued a total of 2,000,000 warrants to the Note Holders as consideration for restructuring of their existing promissory notes.  The warrants were valued using the Black-Scholes option pricing model resulting in a total value of $137,995 which was recorded as deferred financing costs on the Balance Sheet. During the three months ended March 31, 2014, the Company recorded $13,022 in amortization of deferred financing costs. In connection with the conversion to equity of the notes and accrued interest, the Company recorded $101,852, the remaining unamortized costs, as an adjustment to additional paid in capital.
 
6.
Net Loss per Common Share

Basic net loss per common share is calculated by dividing the net loss by the weighted average number of common shares outstanding during the period. Diluted earnings per share is calculated using the weighted average number of common shares outstanding plus dilutive common stock equivalents outstanding during the period. Common stock equivalents are excluded for the three month periods ended March 31, 2014 and 2013, since the effect is anti-dilutive due to the Company’s net losses. Common stock equivalents include stock options and warrants.
 
Basic weighted average common shares outstanding, and the potentially dilutive securities excluded from loss per share computations because they are anti-dilutive, are as follows as of March 31, 2014 and 2013, respectively:
 
   
Three Month Period Ended March 31,
 
   
2014
   
2013
 
Basic and diluted weighted average common stock shares outstanding
    5,568,802       4,990,971  
Potentially dilutive securities excluded from loss per share computations:
               
Common stock options
    1,370,465       1,419,553  
Common stock purchase warrants
    7,428,141       551,339  

 
9

 

7.
Commitments & Contingencies

Legal Proceedings

We are a party in a number of legal matters filed in the state of New York by the Company or John G. Baust, the Company’s former Chief Executive Officer, and members of his extended family, that are described more fully in the Company’s Annual Report on Form 10-K for the year ended December 31, 2013.  During the three months ended March 31, 2014, there were no significant developments related to these complaints.  We have not made any accrual related to future litigation outcomes as of March 31, 2014 and December 31, 2013.

Leases

In November of 2012 we signed an amended lease agreement, which expanded the premises leased by the Company from the landlord to approximately 26,000 rentable square feet. The term of the lease was extended to July 31, 2021. The amendment includes two (2) options to extend the term of the lease, each option is for an additional period of five (5) years, with the first extension term commencing, if at all, on August 1, 2021, and the second extension term commencing, if at all, immediately following the expiration of the first extension term. In accordance with the amended lease agreement, our monthly base rent increased to approximately $46,000 effective August 1, 2013, with scheduled annual increases each August. The Company is also required to pay an amount equal to the Company’s proportionate share of certain taxes and operating expenses.
 
Employment agreements
 
We have employment agreements with the Chief Executive Officer, Chief Financial Officer, Chief Technology Officer, and Chief Operating Officer which automatically renew for successive one year periods in the event either party does not send the other a “termination notice” not less than 90 days prior to the expiration of the initial term or any subsequent term. The agreements provide for certain minimum compensation per month and incentive bonuses. Under certain conditions, we may be required to continue to pay the base salary and certain other amounts under the agreement for a period of up to two years.
 
 
10

 
 
Item 2.   Management’s Discussion and Analysis of Financial Condition and Results of Operations
 
Forward Looking Statements

The statements contained in this Quarterly Report on Form 10-Q, including under the section titled “Management’s Discussion and Analysis of Financial Condition and Results of Operations,” include forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), including, without limitation, statements regarding BioLife Solutions, Inc. ("BioLife” or the “Company”) management’s expectations, hopes, beliefs, intentions or strategies regarding the future. The words “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “plan” and similar expressions may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. The forward-looking statements contained in this Quarterly Report on Form 10-Q are based on the Company’s current expectations and beliefs concerning future developments and their potential effects on the Company. There can be no assurance that future developments affecting the Company will be those that it has anticipated. These forward-looking statements involve a number of risks, uncertainties or other assumptions that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include those factors described in greater detail in the risk factors disclosed in our Form 10-K for the fiscal year ended December 31, 2013 filed with the SEC. Should one or more of these risks or uncertainties materialize, or should any of our assumptions prove incorrect, actual results may vary in material respects from those anticipated in these forward-looking statements. The Company undertakes no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required under applicable securities laws.

Overview

Management’s discussion and analysis provides additional insight into the Company and is provided as a supplement to, and should be read in conjunction with, our annual report on Form 10-K for the fiscal year ended December 31, 2013 filed with the SEC.

BioLife was originally incorporated in Delaware in 1987 under the name Trans Time Medical Products, Inc. In 2002, the Company, then known as Cryomedical Sciences, Inc., and engaged in manufacturing and marketing cryosurgical products, completed a merger with our wholly-owned subsidiary, BioLife Solutions, Inc., which was engaged as a life sciences tools provider. Following the merger, we changed our name to BioLife Solutions, Inc. We do not have any subsidiaries.
 
We develop, manufacture and market patented hypothermic storage and cryopreservation solutions for cells and tissue. Our product offerings include:
 
  
Patented biopreservation media products for cells, tissues, and organs
  
Generic formulations of blood stem cell freezing media products
  
Custom product formulation and custom packaging services
  
Precision thermal packaging products
  
Contract aseptic manufacturing formulation, fill, and finish services of liquid media products
 
Our proprietary HypoThermosol® FRS and CryoStor®, generic BloodStor® biopreservation media products and SAVSU®’s precision thermal packaging products are marketed to the biobanking, drug discovery, and regenerative medicine markets, including hospital-based stem cell transplant centers, pharmaceutical companies, cord blood and adult stem cell banks, hair transplant centers, and suppliers of cells to the drug discovery, toxicology testing and diagnostic markets. All of our products are serum-free and protein-free, fully defined, and are manufactured under current Good Manufacturing Practices (cGMP) using United States Pharmacopia (USP)/Multicompendial or the highest available grade components.
 
Our patented biopreservation media products are formulated to reduce preservation-induced, delayed-onset cell damage and death. Our platform enabling technology provides our customers significant shelf life extension of biologic source material and final cell products, and also greatly improved post-preservation cell, tissue, and organ viability and function. We believe that our products have been incorporated into the manufacturing, storage, shipping, freezing, and clinical delivery processes of over 100 hospital-approved or clinical trial stage regenerative medicine applications.
 
The discoveries made by our scientists and consultants relate to how cells, tissues, and organs respond to the stress of hypothermic storage, cryopreservation, and the thawing process. These discoveries enabled the formulation of innovative biopreservation media products that protect biologic material from preservation-related cellular injury, much of which is not apparent immediately after return to normothermic body temperature. Our product formulations have demonstrated notable reduction in apoptotic (programmed) and necrotic (pathologic) cell death mechanisms and are enabling the clinical and commercial development of dozens of innovative regenerative medicine products.
 
 
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Results of Operations

Recent Developments

Reverse Stock Split
 
On January 17, 2014, our Board of Directors approved an amendment to our certificate of incorporation to effect a reverse stock split by a ratio of 1 for 14, with no reduction in the number of shares of common stock that were previously authorized in our certificate of incorporation.  The reverse stock split was effective on January 29, 2014.  Unless otherwise noted, all share and per share data in this annual report give effect to the 1-for-14 reverse stock split of our common stock.
 
Public Offering of Units
 
On March 25, 2014, we closed a registered public offering of 3,588,878 units for gross proceeds of $15,432,175. Each unit consisted of one share of the Company’s common stock and one warrant, each warrant exercisable for seven years to purchase one share of the Company’s common stock at an exercise price of $4.75. Net of placement agent fees of $1,211,734 and offering costs of $624,211, we received net proceeds of $13,596,230.
 
Conversion of Notes and Interest to Equity
 
Pursuant to previously disclosed note conversion agreements with WAVI Holding AG and Taurus4757 GmbH (the “Note Holders”), concurrently with the closing of the Company’s public offering of units, the Company converted approximately $14.3 million of indebtedness, including accrued interest, to the Note Holders into equity, issuing to the Note Holders an aggregate of 3,321,405 units having terms substantially similar to the public offering units.  In connection with the note conversion, the Company’s $14.3 million indebtedness to the Note Holders under the terms of the Company’s previously disclosed facility agreements were extinguished, all remaining unamortized deferred finance costs were recorded to additional paid in capital, and the Note Holders agreed to release all security interests.
 
Listing of Common Stock on NASDAQ Capital Market
 
On March 26, 2014, our common stock was listed on the Nasdaq Capital Market under the symbol BLFS.
 
Contract Manufacturing Services
 
We completed manufacturing products for the most recent purchase order from our contract manufacturing services customer  in April of 2014. Subsequently, we were informed that this customer does not intend to issue us any significant new purchase orders. We have not received any notice of termination of the manufacturing services ageement nor any breach of performance and we believe that we have met all of the performance requirements in the manufacturing services agreement with this customer.
 
Since the Company expects no further significant business from this customer and to enable the broadest operating freedom, on On May 8, 2014, we provided this customer with notice of termination of the agreement dated December 22, 2011.  The agreement’s termination is anticipated to be effective on or about November 5, 2014, which is 180 days after the date of our notice.  The agreement bars us from manufacturing or selling any solution that is approved for clinical use related to the storage and transportation of human organs for a period of two years after termination (the “tail period”). We do not expect the tail period restrictions to affect our core proprietary business or our ability to pursue other non-conflicting contract manufacturing opportunities in any way.
 
Launch of biologistexSM
 
At the 20th ISCT Annual Meeting, we announced the planned launch of biologistex, a new integrated platform of a cloud-based information service and precision thermal shipping products for cells and tissues, together with SAVSU Technologies, Inc. (“SAVSU”). We anticipate that the biologistex family of products will include next generation controlled temperature transport containers from SAVSU, branded as EVO™. The reusable, highly durable EVO shippers will require little to no maintenance and are available in two configurations, designed to maintain cell and tissue payloads for multiple days at 2-8°C or near -80°C. We anticipate that biologistex products will be marketed to BioLife’s strategic markets including regenerative medicine, pharmaceutical, and biobanking, as complementary technologies to BioLife’s best in class, clinical grade biopreservation media products.

We are currently working with SAVSU to finalize the financial, technical and legal aspects of the biologistex product line, including whether the products will be owned and marketed by BioLife or by another entity, in which BioLife and SAVSU may hold an interest.  In order to manufacture and sell the biologistex line of products, we will need to successfully conclude our discussions with SAVSU.
 
 
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Other Significant Achievements for the First Quarter of 2014
 
  
The United States Patent and Trademark Office issued the Company a new patent on February 4, 2014. Patent number 8,642,255, titled “MATERIALS AND METHODS FOR HYPOTHERMIC COLLECTION OF WHOLE BLOOD”, includes claims related to hypothermic preservation and storage of whole blood and blood components using the Company’s HypoThermosol cell and tissue storage/shipping medium.

  
We announced that Natick, Massachusetts-based Parcell Laboratories has adopted BioLife’s CryoStor clinical grade cell and tissue freeze media for use in future clinical trials of Early Lineage Adult (ELA) stem cell-potential therapies, for which Parcell holds an exclusive worldwide license.

  
Adaptimmune Ltd adopted the Company’s CryoStor clinical grade cell and tissue freeze media for use in Adaptimmune’s current phase I/II clinical trial CT Antigen TCR-Engineered T Cells for Myeloma. With this announcement, Adaptimmune joined the growing list of BioLife customers developing adoptive immunotherapies for various cancers. The cancer immunotherapy field was selected by the editors of Science magazine as the Breakthrough of the Year for 2013.
 
Comparison of Results of Operations for the Three Month Periods Ended March 31, 2014 and 2013

Percentage comparisons have been omitted within the following table where they are not considered meaningful.

Revenue and Gross Margin

   
Three Month Period Ended
     
   
March 31,
     
   
2014
   
2013
   
% Change
 
Revenue:
                       
Core product sales
 
$
1,132,245
   
$
770,133
     
47%
 
Contract manufacturing services
   
932,785
     
780,712
     
19%
 
Licensing revenue
   
––
     
609,167
     
(100)%
 
Total revenue
   
2,065,030
     
2,160,012
     
(4)%
 
                         
Cost of sales
   
1,161,641
     
1,034,528
     
12%
 
Gross profit
 
$
903,389
   
$
1,125,484
     
  (20)%
 
Gross margin %
   
44%
     
52%
         
 
Core Product Sales. Our core products are sold through both direct and indirect channels. Sales to our core customers in the three months ended March 31, 2014 increased by 33% due to a 42% increase in liters sold and a 3% increase in our average selling price per liter over the same period in 2013. Sales to our core customers tend to be uneven due to the pace of product evaluation, adoption, and clinical trials. Management believes that our opportunity in the regenerative medicine market will start to become fully realized over the next three to five years as some customers receive regulatory and marketing approvals for their clinical cell and tissue-based products. We continue to have a goal for 2014 of increasing our core product sales at a rate of 25-35% over 2013. Our 2014 core product sales will depend on a number of factors, including the level and pace of market adoption of our products; the clinical and commercial success of our customers; competition; and the risks set forth in our annual report on Form 10-K under the heading “Risk Factors”. No assurance can be provided that we will achieve our product sales goal.

Contract Manufacturing Services. Contract manufacturing services represents sales of product to one significant customer, ORS. Contract manufacturing services revenue increased in the three months ended March 31, 2014 compared to the same period in 2013 due primarily to more product being produced and delivered to this customer in 2014 compared to 2013.
 
We expect to record revenue of approximately $0.1 million related to the remainder of the most recent purchase order in the second quarter of 2014, and no further revenue subsequent to that. Based on our historical run rate of revenue and costs, assuming this customer would otherwise have generated an additional $3 million in contract manufacturing revenue during the year ended December 31, 2014, the loss of this customer is expected to result in a reduction in gross profit of approximately $0.3 million and non-absorption of up to $0.7 million in certain manufacturing overhead costs for the year ending December 31, 2014. The financial effect on the Company of this contract termination may be mitigated if the related overhead costs can be reduced or reallocated to other products, such as our existing or new core products or new contract manufacturing relationships. In contrast, expect an increase in overall gross margin percentage reflecting the reduction in materials and supplies required to manufacture the contract manufactured product.
 
 
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Licensing Revenue. During the first quarter of 2013, we negotiated a new intellectual property license agreement that provides one customer with limited access to our intellectual property under certain conditions. This customer paid upfront fees for the specific rights and there are no future performance obligations. The upfront fee of $500,000 was recognized as revenue during the quarter and $109,167 in deferred revenue associated with this customer was recognized as all future performance obligations associated with the previous license agreements were cancelled with the agreement signed in the first quarter of 2013.
 
Cost of Sales. Cost of sales consists of raw materials, labor and overhead expenses.  Cost of sales in the three months ended March 31, 2014 increased compared to the same periods in 2013 due primarily to the significant increase in volume in our core business as well as increased sales to our contract manufacturing services customer.
 
Gross Margin. Gross margin as a percentage of revenue was 44% in the three months ended March 31, 2014 compared to 52% in the three months ended March 31, 2013. Gross margin as a percentage of revenue in the three months ended March 31, 2013 included the impact of recognition of significant license revenue during the quarter with no associated costs, which resulted in a significant improvement in gross margin as a percentage of revenue in the first quarter of 2013. Excluding the impact of the license revenue, gross margin as a percentage of revenue increased for the three months ended March 31, 2014 compared to the same period in 2013 primarily due to the significant increase in core product sales, which has a higher gross margin, compared to a lesser increase in contract manufacturing services in 2014, compared to 2013.
 
Operating Expenses

Our operating expenses for the three month periods ended March 31, 2014 and 2013 were:

   
Three Month Period Ended
     
   
March 31,
     
   
2014
   
2013
   
% Change
 
Operating Expenses:
                       
     Research and development
 
$
167,287
   
$
105,968
     
58%
 
     Sales and marketing
   
241,400
     
202,758
     
19%
 
     General and administrative
   
863,742
     
624,427
     
38%
 
Operating Expenses
   
1,272,429
     
933,153
     
36%
 
      % of revenue
   
62%
     
43%
         

Research and Development. Research and development expenses consist primarily of salaries and other personnel expenses, consulting and other outside services including legal services, laboratory supplies, and other costs.  We expense all research and development costs as incurred.  Research and development expenses for the three months ended March 31, 2014 increased compared to the same period in 2013 primarily due to higher spending on legal costs related to patent renewal and consulting and supplies related to the development of new products.
 
Sales and Marketing. Sales and marketing expenses consist primarily of salaries and other personnel-related expenses, consulting, trade shows and advertising.  The increase in the three months ended March 31, 2014 compared to the same period in 2013 was due primarily to higher spending on trade shows and conferences and higher personnel costs.
 
General and Administrative Expenses. General and administrative expenses consist primarily of salaries and other personnel-related expenses, non-cash stock-based compensation for administrative personnel and non-employee members of the board of directors, professional fees, such as accounting and legal, corporate insurance and facilities costs.  The increase in general and administrative expenses in the three months ended March 31, 2014 compared to the same period in 2013 was due primarily to higher corporate costs, including higher corporate insurance, directors’ fees, legal fees and accounting fees, plus higher consulting fees for investor relations.
 
Other Income (Expenses)

Interest Expense. The reduction in interest expense in the three months ended March 31, 2014 compared to the same period in 2013 is due to the conversion of the notes and interest through March 25, 2014, and did not include a full quarter of interest. See above, “Results of Operations - Recent Developments - Conversion of Notes and Interest to Equity.”
 
 
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Amortization of Deferred Financing Costs. During the three months ended March 31, 2014, the Company recorded $13,022 in amortization of deferred financing costs. In connection with the termination of the note facility agreements, the Company recorded $101,852, the remaining unamortized costs, as an adjustment to additional paid in capital. See above, “Results of Operations - Recent Developments - Conversion of Notes and Interest to Equity.”
 
Liquidity
 
We believe that our current level of cash and cash equivalents will be sufficient to meet our liquidity needs for the foreseeable future. We expect to have ongoing cash requirements which we plan to fund through total available liquidity and cash flows generated from operations. Our future uses of cash, which may vary from time to time based on market conditions and other factors, are centered around growing our core business, and continuing to strengthen our balance sheet and competitive position.
 
Our liquidity plans are subject to a number of risks and uncertainties, including those described in the “Risk Factors” section of our Annual Report on Form 10-K for the year ended December 31, 2013, as filed with the SEC on February 12, 2014, some of which are outside our control. Macroeconomic conditions could limit our ability to successfully execute our business plans and therefore adversely affect our liquidity plans.
 
We continue to monitor and evaluate opportunities to strengthen our balance sheet and competitive position over the long-term. These actions may include the possibility of acquisitions or strategic alliances that we believe would generate significant advantages and substantially strengthen our business.
 
On March 31, 2014, we had $12,839,600 in cash and cash equivalents, compared to cash and cash equivalents of $156,273 at December 31, 2013.
 
Net Cash Used In Operating Activities
 
During the three months ended March 31, 2014, net cash used in operating activities was $894,126 compared to $126,476 for the three months ended March 31, 2013.  Cash used in operating activities increased primarily due to the use of cash to fund a higher net loss in 2014 compared to 2013 and payment in the first quarter of 2014 of accrued compensation and other liabilities that were accrued at the end of 2013.
 
Net Cash Used in Investing Activities
 
Net cash used in investing activities totaled $18,777 and $33,937 during the three months ended March 31, 2014 and 2013, respectively. Cash used in investing activities was primarily due to the purchase of equipment.
 
Net Cash Provided by Financing Activities
 
Net cash provided by financing activities of $13,596,230 in the three months ended March 31, 2014 represents gross proceeds of $15,432,175 received in the registered public stock offering completed on March 25, 2014, net of placement agent fees of $1,211,735 and offering costs of $624,211. Net cash provided by financing activities of $25,458 during the three months ended March 31, 2013 was the result of proceeds received from warrant and employee stock option exercises.
 
Upon conversion of all of our outstanding notes and interest to equity on March 25, 2014, we terminated the facility agreements.
 
Off-Balance Sheet Arrangements
 
As of March 31, 2014, we did not have any off-balance sheet arrangements.
 
Critical Accounting Policies and Significant Judgments and Estimates
 
Management’s discussion and analysis of our financial condition and results of operations is based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States. The preparation of financial statements requires that we make estimates and assumptions that affect the reported amounts of assets and liabilities and the disclosure of contingent assets and liabilities at the date of the financial statements as well as reported revenues and expenses during the reporting periods. On an ongoing basis, we evaluate estimates, including, but not limited to those related to accounts receivable allowances, determination of fair value of share-based compensation, contingencies, income taxes, and expense accruals. We base our estimates on historical experience and on other factors that we believes are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ materially from these estimates under different assumptions or conditions.
 
 
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Our critical accounting policies and estimates have not changed significantly from those policies and estimates disclosed under the heading “Critical Accounting Policies and Significant Judgments and Estimates” in Part II, Item 7, “Management’s Discussion and Analysis of Financial Conditions and Results of Operations” of our Annual Report on Form 10-K for the fiscal year ended December 31, 2013, filed with the SEC.
 
Contractual Obligations
 
We previously disclosed certain contractual obligations and contingencies and commitments relevant to us within the financial statements and Management Discussion and Analysis of Financial condition and Results of Operations in our Annual report on Form 10-K for the year ended December 31, 2013, as filed with the SEC on February 12, 2014. There have been no material changes to the disclosure under the heading “Contractual Obligations” in Part II, Item 7, “Management’s Discussion and Analysis of Financial Condition and Results of Operations” of our 2013 Annual Report on Form 10-K. for more information regarding our current contingencies and commitments, see note 7 to the financial statements included above.
 
Item 3.   Quantitative and Qualitative Disclosures about Market Risk
 
Not applicable.
 
Item 4.   Controls and Procedures

Evaluation of Disclosure Controls and Procedures. We maintain disclosure controls and procedures that are designed to ensure that material information required to be disclosed in our periodic reports filed under the Exchange Act is recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms and to ensure that such information is accumulated and communicated to our management, including our chief executive officer and chief financial officer as appropriate, to allow timely decisions regarding required disclosure. During the quarter ended March 31, 2014, we carried out an evaluation, under the supervision and with the participation of our management, including the chief executive officer and chief financial officer, as required by the rules and regulations under the Exchange Act, of the effectiveness of the design and operation of our disclosure controls and procedures, as defined in Rule 13a-15(e) and 15d-15(e) under the Exchange Act. Based on this evaluation, our chief executive officer and chief financial officer concluded that, as of March 31, 2014, our disclosure controls and procedures were effective.

Changes in Internal Control over Financial Reporting. There have been no changes in our internal control over financial reporting (as defined in Rule 13a-15(f) and 15d-15(f) under the Exchange Act) that occurred during the quarter ended March 31, 2014 that have materially affected or are reasonably likely to materially affect our internal control over financial reporting.

Limitations on Effectiveness of Control. Our management, including our chief executive officer and chief financial officer, does not expect that our disclosure controls and procedures or our internal controls over financial reporting will prevent all errors and all fraud. A control system, no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. Further, the design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, within our Company have been detected.

 
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PART II:  Other Information

Item 5.    Other Information

The information set forth in Part I, Item 2, under the heading “Results of Operations – Recent Developments – Contract Manufacturing Agreement” is incorporated herein by reference.
 
Item 6.    Exhibits
 
See accompanying Index to Exhibits included after the signature page of this report for a list of exhibits filed or furnished with this report.

 
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SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the Registrant has duly caused this Report to be signed on its behalf by the undersigned, thereunto duly authorized.
 
         
       
BIOLIFE SOLUTIONS, INC.
     
Dated: May 8, 2014
     
/s/ Daphne Taylor
       
Daphne Taylor
       
Chief Financial Officer
(Duly authorized officer and principal financial and accounting officer)
                                                                                                    
 
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BIOLIFE SOLUTIONS, INC.

INDEX TO EXHIBITS
 
Exhibit No.
 
Description
     
4.1
 
Form of Warrant issued to purchasers in the Public Offering (incorporated by reference to Exhibit 4.1 to the Company’s report on Form 8-K filed March 20, 2014)
     
4.2
 
Form of Warrant issued to Note Holders in the Note Conversion (incorporated by reference to Exhibit 10.1 to the Company’s report on Form 8-K filed March 25, 2014)
     
10.1
 
Placement Agent Agreement, dated March 20, 2014, BioLife Solutions, Inc. and Ladenburg Thalmann & Co. Inc. (incorporated by reference to Exhibit 10.1 to the Company’s report on Form 8-K filed March 20, 2014)
     
10.2
 
Form of Securities Purchase Agreement (incorporated by reference to Exhibit 10.2 to the Company’s report on Form 8-K filed March 20, 2014)
     
 
Certification pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
     
 
Certification pursuant to Section 302 of the Sarbanes-Oxley Act of 2002
     
 
Certification pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
     
 
Certification pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
 
*Filed herewith
 
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