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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Form 10-Q
(Mark One)
[X] Quarterly Report Pursuant to Section 13 or 15(d) of the Securities Exchange
Act of 1934
For the quarterly period ended March 31, 1999, or
[ ] 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 000-21615
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BOSTON BIOMEDICA, INC.
(Exact name of Registrant as Specified in its Charter)
Massachusetts 04-2652826
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(State or other (I.R.S. Employer
Jurisdiction of Identification No.)
Incorporation or
Organization)
375 West Street,
West Bridgewater,
Massachusetts 02379-1040
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(Address of Principal (Zip Code)
Executive Offices)
Registrant's telephone number, including area code (508) 580-1900
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Indicate by check 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 [X] No [ ]
The number of shares outstanding of the Registrant's only class of common
stock as of April 30, 1999 was 4,717,816.
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Part I. Financial Information
Item 1. Financial Statements
BOSTON BIOMEDICA, INC. AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
For the Three Months Ended
March 31,
----------------------------
1999 1998
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REVENUE:
Products $ 3,456,202 $ 3,063,359
Services 3,388,963 3,209,436
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Total revenue 6,845,165 6,272,795
COSTS AND EXPENSES:
Cost of product sales 1,808,647 1,771,751
Cost of services 2,470,097 2,323,211
Research and development 762,609 432,389
Acquired research and development - 850,000
Selling and marketing 1,005,271 928,612
General and administrative 1,094,690 1,029,936
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Total operating costs and expenses 7,141,314 7,335,899
Loss from operations (296,149) (1,063,104)
Interest income 696 24,530
Interest expense (87,199) (971)
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Loss before income taxes (382,652) (1,039,545)
Benefit from income taxes 145,408 395,027
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Net loss $ (237,244) $ (644,518)
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Net loss per share, basic $ (0.05) $ (0.14)
Net loss per share, diluted $ (0.05) $ (0.14)
Number of shares used to calculate net loss per share
Basic 4,717,816 4,632,061
Diluted 4,717,816 4,632,061
The accompanying notes are an integral part of the Consolidated Financial
Statements
2
BOSTON BIOMEDICA, INC. AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
(Unaudited)
March 31, December 31,
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1999 1998
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ASSETS
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CURRENT ASSETS:
Cash and cash equivalents $ 113,286 $ 146,978
Accounts receivable, less allowances of $632,281 in 1999 and
$623,710 in 1998 6,151,929 6,086,693
Inventories 6,662,708 6,689,768
Prepaid expense and other 731,678 479,983
Deferred income taxes 842,407 847,268
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Total current assets 14,502,008 14,250,690
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Property and equipment, net 7,090,702 6,925,423
OTHER ASSETS:
Goodwill and other intangibles, net 2,754,635 2,809,825
Notes receivable and other 92,548 96,447
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2,847,183 2,906,272
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TOTAL ASSETS $ 24,439,893 $ 24,082,385
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LIABILITIES AND STOCKHOLDERS' EQUITY
------------------------------------
CURRENT LIABILITIES:
Accounts payable $ 1,932,434 $ 2,369,495
Accrued compensation 1,013,391 1,284,162
Other accrued expenses 675,225 795,642
Current maturities of long term debt 15,951 15,569
Deferred revenue 690,760 690,760
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Total current liabilities 4,327,761 5,155,628
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LONG-TERM LIABILITIES:
Long term debt, less current maturities 5,307,702 3,988,602
Other liabilities 686,971 730,138
Deferred income taxes 137,612 139,363
STOCKHOLDERS' EQUITY:
Common stock, $.01 par value; authorized 20,000,000 shares in
1999 and 1998; issued and outstanding 4,717,816 in 1999 and
4,667,816 in 1998 47,178 46,678
Additional paid-in capital 16,566,654 16,418,717
Retained earnings (2,633,985) (2,396,741)
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Total stockholders' equity 13,979,847 14,068,654
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TOTAL LIABILITIES & STOCKHOLDERS' EQUITY $ 24,439,893 $ 24,082,385
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The accompanying notes are an integral part of the Consolidated Financial
Statements
3
BOSTON BIOMEDICA, INC. AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited)
For the Three Months Ended
March 31,
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1999 1998
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CASH FLOWS FROM OPERATING ACTIVITIES:
Net loss $ (237,244) $ (644,518)
Adjustments to reconcile net loss to net
cash (used in) provided by operating activities:
Depreciation and amortization 352,911 326,890
Provision for doubtful accounts (8,005) 50,756
Deferred rent and other liabilities (43,167) 137,441
Deferred income taxes 3,110 (21,937)
Acquired research and development - 850,000
Changes in operating assets and liabilities:
Accounts receivable (57,231) 607,845
Inventories 27,060 (475,762)
Prepaid expenses (251,695) (496,483)
Accounts payable (437,061) (266,116)
Accrued compensation and other expenses (391,188) (319,099)
Deferred revenue - (275,835)
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Net cash used in operating activities (1,042,510) (526,818)
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CASH FLOWS FROM INVESTING ACTIVITIES:
Acquired research and development - (850,000)
Additions to property and equipment (463,000) (803,655)
Advances under notes receivable and other assets 3,899 11,950
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Net cash used in investing activities (459,101) (1,641,705)
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CASH FLOWS FROM FINANCING ACTIVITIES:
Proceeds from long term debt 1,335,051 -
Repayments of long-term debt (15,569) (403)
Proceeds of common stock issued 148,437 39,250
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Net cash provided by financing activities 1,467,919 38,847
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DECREASE IN CASH AND CASH EQUIVALENTS: (33,692) (2,129,676)
Cash and cash equivalents, beginning of period 146,978 2,772,360
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Cash and cash equivalents, end of period $ 113,286 $ 642,684
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The accompanying notes are an integral part of the Consolidated Financial
Statements
4
BOSTON BIOMEDICA, INC. AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(1) Basis of Presentation
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The accompanying unaudited consolidated financial statements have been
prepared in accordance with generally accepted accounting principles for the
interim financial information and with the instructions to Form 10-Q and Article
10 of Regulation S-X. Accordingly, they do not include all of the information
and footnotes required by generally accepted accounting principles for complete
financial statements. In the opinion of management, all adjustments (consisting
of only normal recurring adjustments) considered necessary for a fair
presentation have been included. Operating results for the three months ended
March 31, 1999 are not necessarily indicative of the results that may be
expected for the year ending December 31, 1999. For further information, refer
to the consolidated financial statements and footnotes thereto included in the
Form 10-K filing for the fiscal year ended December 31, 1998 for Boston
Biomedica, Inc. and Subsidiaries ("the Company" or "Boston Biomedica"). Certain
prior years' amounts in the consolidated financial statements may have been
reclassified to conform to the current year's presentation.
(2) Use of Estimates
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In conformity with generally accepted accounting principles, management is
required to make estimates and assumptions that affect the reported amounts of
assets, liabilities, revenues, and expenses for the periods presented. Such
estimates include reserves for uncollectable accounts receivable as well as the
net realizable value of its inventory. Actual results could differ from the
estimates and assumptions used by management.
(3) Inventories
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Inventories consisted of the following:
March 31, December 31,
1999 1998
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Raw materials .............................. $2,330,396 $2,407,154
Work-in-process ............................ 2,044,748 1,788,399
Finished goods ............................. 2,287,564 2,494,215
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$6,662,708 $6,689,768
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(4) Segment Reporting and Related Information (all dollar amounts in thousands)
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Selected summarized results for the Company's four operating segments are
as follows:
March 31,
Segment revenue: 1999 1998
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Diagnostics $ 3,923 $ 3,619
Clinical Laboratory Services 2,205 1,587
Laboratory Instrumentation 1,034 1,198
Other - -
Eliminations (317) (131)
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Total Revenue $ 6,845 $ 6,273
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March 31,
Segment operating (loss) income: 1999 1998
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Diagnostics $ 145 $ (52)
Clinical Laboratory Services 146 69
Laboratory Instrumentation (133) (198)
Other (454) (32)
Acquired R&D - (850)
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Total (Loss) Income from Operations $ (296) $ (1,063)
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5
BOSTON BIOMEDICA, INC. AND SUBSIDIARIES
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(4) Segment Reporting and Related Information (Continued)
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March 31, Dec. 31,
Identifiable segment assets: 1999 1998
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Diagnostics $ 16,403 $ 16,548
Clinical Laboratory Services 2,629 2,348
Laboratory Instrumentation 4,427 4,428
Other 981 758
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Total assets $ 24,440 $ 24,082
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(5) Acquired Research and Development
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In March 1998, the Company acquired from BioSeq, Inc.("BioSeq"), the sole
and exclusive worldwide right to development stage technology, including the use
of BioSeq technical information, licensed processes and improvements to develop,
manufacture, market and sell or sublicense products or services in the field of
human in vitro immunodiagnostics. In accordance with accounting standards for
purchased research and development, costs totaling $850,000 were expensed in
that period. In September, 1998 the Company acquired 100% of the remaining stock
of BioSeq in a purchase transaction. See also the Company's most recent filing
on Form 10-K for the year ended December 31, 1998.
(6) Computation of Net Income per Share
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In February 1997, the Financial Accounting Standards Board issued Statement
of Financial Accounting Standards ("SFAS") No. 128, "Earnings per Share". SFAS
128 establishes a different method of computing net income per share than was
required under the provisions of the previous standard-Accounting Principles
Board opinion No. 15. The following illustrates the computation of basic and
diluted net income per share.
Quarter Ended March 31,
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1999 1998
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Shares, basic 4,717,816 4,632,061
Net effect of dilutive common stock
equivalents-based on treasury stock
method using average market price * - -
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Shares, diluted 4,717,816 4,632,061
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Net loss, basic and diluted $ (237,244) $ (644,518)
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Net loss per share-basic (0.05) (0.14)
Net loss per share-diluted (0.05) (0.14)
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* Potentially dilutive securities of 107,598 and
246,148 were not included in the computation of
diluted earnings per share because to do so would
have reduced the loss per share for the three months
ended March 31, 1999 and 1998, respectively.
6
Item 2. Management's Discussion and Analysis of Results of Operations and
Financial Condition.
Three Months Ended March 31, 1999 and 1998
Total revenue increased 9.1%, or $572,000, to $6,845,000 for the quarter
ended March 31, 1999 from $6,273,000 in the prior year period. This increase was
the result of an increase in product sales of 12.8%, or $393,000, to $3,456,000
from $3,063,000 and an increase in service revenue of 5.6%, or $180,000, to
$3,389,000 from $3,209,000. The increase in product revenue was primarily the
result of an overall sales increase of 9.4% in Quality Control Products, due to
continued strong sales of Accurun(R) and custom (OEM) panel products, partially
offset by a decline in seroconversion panel sales as a result of fewer ongoing
development programs in the in vitro diagnostic test kit industry. Laboratory
instruments also showed a significant increase in revenue, primarily related to
contract manufacturing. The increase in service revenue was primarily
attributable to the continued growth in nucleic acid (molecular) testing, and
immunological testing, partially offset by a decline in service revenue at our
Laboratory Instrumentation segment as the previously announced ABX modified
contract winded down to completion in the first quarter of 1999.
Gross profit increased 17.8% or $388,000, to $2,566,000 for the current
quarter from $2,178,000 in the prior year period. Product gross profit increased
27.6% or $356,000 to $1,648,000 in 1999 from $1,292,000 in the prior year
quarter, and product gross profit margin increased to 47.7% of revenue in 1999
from 42.2%. This increase was primarily the result of stronger sales of
laboratory instruments in 1999, while fixed costs remained relatively constant,
resulting in higher margins. Service gross profit increased 3.7% or $33,000 to
$919,000 in 1999 from $886,000 in the prior year, as margins remained relatively
steady, declining slightly to 27.1% in 1999 from 27.6% in 1998, on the modest
revenue increase discussed above.
Research and development expenses increased 76.4%, or $330,000, to $762,000
for the current quarter from $432,000 in the prior year period. The increase
relates to development work on the Company's pressure cycling technology
("PCT"), and increased expenditures in its drug discovery program.
There was a one time accounting charge of $850,000 for the quarter ended
March 31, 1998 related to the acquisition of the worldwide exclusive rights to
BioSeq, Inc.'s immunodiagnostic research and development technology.
Selling and marketing expenses increased 8.3%, or $77,000, to $1,005,000
for the current quarter from $928,000 in the prior year period. This increase
was primarily attributable to increased personnel costs and marketing expenses.
General and administrative expenses increased 6.3%, or $65,000, to
$1,095,000 for the current quarter from $1,030,000 in the prior year period.
This increase was primarily a result of increased investor relations activities.
The Company generated an operating loss of ($296,000) for the current
quarter versus a loss of ($1,063,000) in the prior year period. The decreased
loss was primarily a result of the above mentioned one time accounting charge in
1998's first quarter.
Net interest expense of ($87,000) was incurred in 1999 versus an income of
$23,000 for the prior year period. The Company completed significant investment
in technology and infrastructure during the first half of 1998, thereby
utilizing its cash available to invest. Since mid 1998, capital expenditures
have been funded primarily through the Company's line of credit.
The Company recorded a tax benefit in both quarters based on the combined
federal and state statutory rate of 38%.
7
Liquidity and Financial Condition
At March 31, 1999, the Company has cash and cash equivalents of
approximately $113,000 and working capital of $10,176,000. Trade accounts
receivable increased $74,000 or 1% during the quarter as collections lagged
expectations. Inventory decreased $27,000 to $6,663,000 as the Company continued
to focus its efforts on utilizing existing inventory where possible rather than
purchasing raw materials for new products.
The Company has financed its operations to date through cash flow from
operations, borrowings from banks and the sale of its common stock. The Company
expects its cash flow, working capital, and available borrowings under its
revolving line of credit to meet existing operational needs in 1999. The Company
has recently received approval for an increased revolving line of credit of $10
million with more liberal financial covenants, which it expects to meet existing
operational needs for the foreseeable future. This facility will be collaterized
by substantially all assets of the Company (excluding its real estate), with
interest based on prime plus 1/4%
Net cash used in operations for the three months ended March 31, 1999 was
$1,042,000 as compared to $527,000 in the prior year period. This decrease in
cash flow was primarily attributable to slower cash receipts compared to the
prior year.
Cash used in investing activities for the three months ended March 31, 1999
was $459,000 as compared to $1,642,000 in the prior year period. The decrease
compared to the prior year was due primarily to a one time technology purchase
in the first quarter of 1998, and lower expenditures in 1999 for property and
equipment, as the improvements at the Company's Maryland facility were completed
in 1998.
Cash provided by financing activities for the three months ended March 31,
1999 was $1,468,000 as compared to $39,000 in the prior year period. The
increase was primarily related to the increased debt from the company's
revolving line of credit incurred to finance additional working capital needs,
and property and equipment additions.
The Company anticipates significant capital expenditures in 1999 to
continue as it plans to complete renovations to its manufacturing facility in
Massachusetts, as well as implement a fully integrated business information
system ("ERP") at all locations. The Company believes that existing cash
balances, the borrowing capacity available under the revolving line of credit,
and cash generated from operations are sufficient to fund operations and
anticipated capital expenditures in 1999. Except for purchase orders in
connection with the manufacturing expansion and ERP system, there were no
material financial commitments for capital expenditures as of March 31, 1999.
Year 2000 Computer Systems Compliance
The following disclosure is a Year 2000 ("Y2K") readiness disclosure
statement pursuant to the Year 2000 Readiness and Disclosure Act.
Boston Biomedica's Year 2000 program is designed to minimize the
possibility of serious Year 2000 interruption. Possible Year 2000 worst case
scenarios include the interruption of significant parts of the Company's
business as a result of internal business system failure or the failure of the
business systems of its suppliers, distributors or customers. Any such
interruption may have a material adverse impact on the future results of the
Company.
In 1997 the Company decided to significantly upgrade its "business systems"
(all computer hardware and software used to run its businesses including its
operations management, administration and financial systems). Specifications
were developed for desired capabilities, including Year 2000 compliance. In 1998
the Company began assessing its Year 2000 exposure and commenced implementation
of a plan to achieve Year 2000 readiness. Based on its review to date, the
Company believes that its products are Year 2000 compliant.
During the third quarter of 1998, after investigating several alternatives,
implementation of an enterprise resource planning system ("ERP system") was
started at two of the Company's four sites. The
8
vendor has certified that the system is Year 2000 compliant. In April 1999,
business systems at the other two sites were upgraded to Y2K compliant versions
of their existing software at a combined cost of approximately $5,000.
A task force with participants and a site leader at each BBI location has
begun reviewing all other infrastructure areas including communications systems,
building security systems, and embedded technologies in areas such as laboratory
instruments and manufacturing equipment. The Company has also begun to survey
major suppliers, distributors, and customers to determine the status and
schedule for their Year 2000 compliance. To date, no significant issues have
been identified, and the survey is expected to be completed in the third quarter
of 1999. Where it believes that a particular supplier's situation poses
unacceptable risks, the Company plans to identify an alternative source.
The costs of the readiness program for business systems, other
infrastructure areas, and suppliers and distributors are a combination of
incremental external spending and use of existing internal resources. In total,
the Company expects to spend less than $150,000 to achieve readiness, of which
approximately 60% has been expended to date. This amount is based on the costs
to upgrade the existing business systems to Y2K compliant versions, and excludes
the costs of implementing the ERP system which is being implemented for reasons
beyond Y2K compliance.
Milestones and implementation dates and the costs of BBI's Year 2000
readiness program are subject to change based on new circumstances that may
arise or new information becoming available that may change the underlying
assumptions or requirements.
Forward-Looking Statements
This Quarterly Report on Form 10-Q contains forward-looking statements
concerning the Company's financial performance and business operations. The
Company wishes to caution readers of this Quarterly Report on Form 10-Q that
actual results might differ materially from those projected in any
forward-looking statements.
Factors which might cause actual results to differ materially from those
projected in the forward-looking statements contained herein include the
following: inability of the Company to develop the end user market for quality
control products; inability of the Company to integrate the business of Source
Scientific, Inc. into the Company's business; inability of the Company to grow
the sales of Source Scientific, Inc. to the extent anticipated; failure to
obtain the renewal and full funding of contracts with National Institutes of
Health (NIH), National Heart, Lung and Blood Institute (NHLBI) and other
government agencies; the possibility that the Company may not be successful in
commercializing current R&D projects, may not have the resources to complete the
projects, or that the projects may take longer than expected to complete;
inability of the Company to obtain an adequate supply of the unique and rare
specimens of plasma and serum necessary for certain of its products; significant
reductions in purchases by any of the Company's major customers; the
interruption of significant parts of the Company's business as a result of
internal business system failure or the failure of the business systems of its
suppliers, distributors or customers due to the inability of such systems to
properly interpret dates subsequent to December 31, 1999; and the potential
insufficiency of Company resources, including capital, human resources, plant
and equipment and management systems, to accommodate any future growth. Certain
of these and other factors which might cause actual results to differ materially
from those projected are more fully set forth under the caption "Risk Factors"
in the Company's Registration Statement on Form S-1 (SEC File No. 333-10759) and
in its most recent filing on Form 10-K for the year ended December 31, 1998.
9
BOSTON BIOMEDICA, INC.
Part II. Other Information
Item 4. Submission of Matters to a Vote of Security Holders.
None
Item 6. Exhibits and Reports on Form 8K
(a) Exhibits
Exhibit No.
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3.1 Amended and Restated Articles of Organization of the Company**
3.2 Amended and Restated Bylaws of the Company**
4.1 Specimen Certificate for Shares of the Company's Common Stock**
4.2 Description of Capital Stock (contained in the Restated
Articles of Organization of the Company filed as Exhibit 3.1)**
27 Financial Data Schedule
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** In accordance with Rule 12b-32 under the Securities Exchange Act of 1934,
as amended, reference is made to the documents previously filed with the
Securities and Exchange Commission, which documents are hereby
incorporated by reference.
(b) Reports on Form 8K
None
10
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the
Registrant has duly caused this Report to be signed on its behalf by the
undersigned, thereunto duly authorized.
BOSTON BIOMEDICA, INC.
Date: May 14, 1999 By /s/ KEVIN W. QUINLAN
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Kevin W. Quinlan, Chief Financial Officer
(Principal Financial Officer)
11
BOSTON BIOMEDICA, INC.
EXHIBIT INDEX
EXHIBIT INDEX
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Exhibit No. Reference
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3.1 Amended and Restated Articles of Organization of the Company A**
3.2 Amended and Restated Bylaws of the Company A**
4.1 Specimen Certificate for Shares of the Company's Common Stock A**
4.2 Description of Capital Stock (contained in the Restated Articles of A**
Organization of the Company filed as Exhibit 3.1)
27 Financial Data Schedule Filed herewith
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A Incorporated by reference to the Company's Registration Statement on Form
S-1 (Registration No. 333-10759)(the "Registration Statement"). The number
set forth herein is the number of the Exhibit in said registration
statement.
** In accordance with Rule 12b-32 under the Securities Exchange Act of 1934,
as amended, reference is made to the documents previously filed with the
Securities and Exchange Commission, which documents are hereby incorporated
by reference.
12