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| ERES > SEC Filings for ERES > Form 10-Q on 6-Nov-2009 | All Recent SEC Filings |
6-Nov-2009
Quarterly Report
Cautionary Statement for Forward-Looking Information
The following discussion and analysis should be read in conjunction with our
consolidated financial statements and the related notes to the consolidated
financial statements appearing elsewhere in this Form 10-Q. The following
discussion and analysis includes forward-looking statements within the meaning
of the Private Securities Litigation Reform Act of 1995 that reflect our current
views as to future events and financial performance with respect to our
operations. These statements can be identified by the fact that they do not
relate strictly to historical or current facts. They use words such as "aim,"
"anticipate," "are confident," "estimate," "expect," "will be," "will continue,"
"will likely result," "project," "intend," "plan," "believe," "look to" and
other words and terms of similar meaning in conjunction with a discussion of
future operating or financial performance.
These statements are subject to risks and uncertainties that could cause actual
results to differ materially from those expressed or implied in the
forward-looking statements. Factors that might cause such a difference include:
unfavorable economic conditions; our ability to obtain new contracts and
accurately estimate net revenues due to variability in size, scope and duration
of projects and internal issues at the sponsoring client; our ability to
successfully integrate acquisitions; competitive factors in the market for
centralized Cardiac Safety services; changes in the pharmaceutical,
biotechnology and medical device industries to which we sell our solutions;
technological development; and market demand. There is no guarantee that the
amounts in our backlog will ever convert to revenue. Should the current economic
conditions continue or deteriorate further, the cancellation rates that we have
historically experienced could increase. Further information on potential
factors that could affect the Company's financial results can be found in the
reports we file with the Securities and Exchange Commission.
Forward-looking statements speak only as of the date made. We undertake no
obligation to update any forward-looking statements, including prior
forward-looking statements, to reflect the events or circumstances arising after
the date as of which they were made. As a result of these risks and
uncertainties, readers are cautioned not to place undue reliance on any
forward-looking statements included in this discussion or that may be made in
our filings with the Securities and Exchange Commission or elsewhere from time
to time by, or on behalf of, us.
Overview
We were founded in 1977 to provide Cardiac Safety solutions to evaluate the
safety of new drugs. We provide technology and service solutions that enable the
pharmaceutical, biotechnology and medical device industries to collect,
interpret and distribute cardiac safety data more efficiently. We are a market
leader in providing centralized electrocardiographic solutions (Cardiac Safety
solutions) and a provider of technology solutions that streamline the clinical
trials process by enabling our clients to evolve from traditional, paper-based
methods to electronic processing using our ePRO products and solutions.
On June 23, 2009, we completed the sale of certain assets relating to our EDC
operations. Under the terms of the transaction, OmniComm Systems, Inc. issued
8.1 million shares of common stock and assumed certain liabilities including
deferred revenue relating to our EDC operations in exchange for our EDC assets
which primarily included our EDC software, applications and fixed assets and
$1.15 million in cash we paid. During the nine months ended September 30, 2009,
we recorded a gain on the sale of these assets of $0.5 million within general
and administrative expenses in the consolidated statement of operations.
Our services revenues consist primarily of our services offered under our
Cardiac Safety and, to a lesser extent, ePRO™ solutions. Our site support
revenue consists of cardiac safety equipment rentals and sales along with
related supplies and logistics management.
We offer Cardiac Safety solutions, which are utilized by pharmaceutical
companies, biotechnology companies, medical device companies, clinical trial
sponsors and clinical research organizations (CROs) during the conduct of
clinical trials. Our Cardiac Safety solutions include the collection,
interpretation and distribution of electrocardiographic (ECG) data and images
and are performed during clinical trials in all phases of the clinical research
process. The ECG provides an electronic map of the heart's rhythm and structure,
and is performed in most clinical trials. Our Cardiac Safety solutions permit
assessments of the safety of therapies by documenting the occurrence of cardiac
electrical change. Specific trials, such as a Thorough QTc study, focus on the
cardiac safety profile of a compound. Thorough QTc studies are comprehensive
studies that typically are of large volume and short duration and are generally
required by the United States Food and Drug Administration (FDA) under guidance
issued in 2005 by the International Committee on Harmonization (ICH E14). We
also offer site support, which includes the rental and sale of cardiac safety
equipment along with related supplies and logistics management. We also offer
ePRO solutions along with proprietary clinical assessments. We offer the
following products and services on a global basis:
Cardiac Safety. Cardiac Safety solutions, including our EXPERT® technology
platform, provide for workflow-enabled cardiac safety data collection,
interpretation and distribution of electrocardiographic (ECG) data and images as
well as for analysis and cardiologist interpretation of ECGs performed on
research subjects in connection with our clients' clinical trials. EXPERT® is
designed specifically to address global regulatory guidance and technical
standards for digital ECG processing to include digital collection, waveform
measurements and annotations, review and output to the regulatory standard file
format. Also included in Cardiac Safety solutions is FDA XML delivery, which
provides for the delivery of ECGs in a format compliant with the United States
Food and Drug Administration's XML standard for digital ECGs. We also provide
ECG equipment through rental and sales to clients to perform the ECG recordings
and give them means to send such recordings to us. A new portal product, MyStudy
Portal, is now providing sponsors and investigator sites with the ability to
order supplies, gain real time reports and respond to queries via a secure web
portal in lieu of less efficient means such as faxing and telephone calls.
Cardiac Safety Consulting. The centralization of electrocardiograms in clinical
research has become increasingly important to organizations involved in the
development of new drugs. Global regulators each apply their own slightly
different interpretation of the International Conference on Harmonization E14
guidelines and, as a result, sponsors look to their vendors to provide key
scientific input into the overall process. Our cardiac safety consulting service
aids sponsors in the development of protocol synopses, the creation and analysis
of statistical plans as well as the provision of an expert medical report with
regard to the cardiac findings. We are involved in all phases of clinical
development from a consultancy point of view. We offer this service both as a
stand-alone service and integrated with our full suite of Cardiac Safety
solutions.
ePRO. Our electronic patient reported outcome (ePRO) solution is an Interactive
Voice Response (IVR) system that allows subjects to easily and quickly report
data for a clinical trial. Because it can be accessed from a standard phone, our
ePRO system is cost effective while being extremely scalable and suitable from
Phase I through Phase IV. Diaries, screening, recruitment and all clinical
assessments can be completed directly by the subject without requiring clinician
involvement.
Project Assurance. We provide a full spectrum of consulting services for all of
our products that augment the study management and implementation efforts of
clients in support of their clinical research requirements.
Services revenues consist of Cardiac Safety and ePRO services that we provide on
a fee for services basis and are recognized as the services are performed. We
also provide Cardiac Safety consulting services on a time and materials basis
and recognize revenues as we perform the services. Site support revenues are
recognized at the time of sale or over the rental period.
For arrangements with multiple deliverables where the fair value of each element
is known, the revenue is allocated to each component based on the relative fair
values of each element. For arrangements with multiple deliverables where the
fair value of one or more delivered elements is not known, revenue is allocated
to each component of the arrangement using the residual method provided that the
fair value of all undelivered elements is known. Fair values for undelivered
elements are based primarily upon stated renewal rates for future products or
services.
We have recorded reimbursements received for out-of-pocket expenses incurred as
revenue in the accompanying consolidated financial statements.
Revenue is recognized on unbilled services and relates to amounts that are
currently not billable to the customer pursuant to contractual terms. In
general, such amounts become billable in accordance with predetermined payment
schedules, but recognized as revenue as services are performed. Amounts included
in unbilled revenue are expected to be collected within one year and are
included within current assets.
Our former electronic data capture (EDC) business is included in EDC licenses
and services and included license revenue, technology consulting and training
services and software maintenance services. We recognized up-front license fee
revenues under the residual method when a formal agreement existed, delivery of
the software and related documentation occurred, collectability was probable and
the license fee was fixed or determinable. We recognized monthly and annual term
license fee revenues over the term of the arrangement. Hosting service fees were
recognized evenly over the term of the service. We recognized revenues from
software maintenance contracts on a straight-line basis over the term of the
maintenance contract, which was typically twelve months. We provided consulting
and training services on a time and materials basis and recognized revenues as
we performed the services.
Cost of services includes the cost of Cardiac Safety and ePRO services. Cost of
services consists primarily of direct costs related to our centralized Cardiac
Safety services and includes wages, depreciation, amortization, fees paid to
consultants and other direct operating costs. Cost of site support consists
primarily of wages, cardiac safety equipment rent and depreciation, related
supplies, cost of equipment sold, shipping expenses and other direct operating
costs. Selling and marketing expenses consist primarily of wages and incentive
compensation paid to sales personnel, travel expenses and advertising and
promotional expenditures. General and administrative expenses consist primarily
of wages and direct costs for our finance, administrative, corporate information
technology, legal and executive management functions, in addition to
professional service fees and corporate insurance. Research and development
expenses consist primarily of wages paid to our product development staff, costs
paid to outside consultants and other direct costs associated with the
development of our technology.
Costs of our former EDC operations included primarily wages, fees paid to
outside consultants and other direct operating costs related to our software
licensing, consulting and client support functions.
We conduct our operations through offices in the United States (U.S.) and the
United Kingdom (UK). Our international net revenues represented approximately
21% and 18% of total net revenues for the nine months ended September 30, 2008
and 2009, respectively. The majority of our revenues are allocated among our
geographic segments based upon the profit split transfer pricing methodology,
and revenues are generally attributed to the geographic segment where the work
is performed. The profit split methodology equalizes gross margins for each
legal entity based upon its respective direct costs.
Reclassifications
The consolidated financial statements for prior periods have been reclassified
to conform to the current period's presentation. In particular, the revenue and
cost of revenue of our former EDC operations have been reclassified from the
licenses and services categories to the EDC category on the consolidated
statements of operations for all periods presented. Additionally, the remaining
revenues and costs of sales in licenses, related to Cardiac safety reporting and
ePRO subscriptions, were reclassified to the services category on the
consolidated statements of operations for all periods presented as these items
are relatively insignificant.
Results of Operations
Executive Overview
Net revenues were $22.7 million for the third quarter of 2009, a decrease of
$11.2 million or 33.0% from $33.9 million in the third quarter of 2008. The year
over year revenue decline was due to a decline in transaction volumes primarily
in Thorough QTc and to a lesser extent routine studies, lower revenue from
acquired backlog of Covance Cardiac Safety Services, Inc. (CCSS) as this backlog
nears completion and lower equipment sales in the third quarter of 2009 than in
the third quarter of 2008 as more customers chose to rent cardiac safety
equipment. We also sold our EDC operation in June 2009 and accordingly EDC
revenue in the third quarter of 2009 was zero compared to $1.6 million of EDC
revenue in the third quarter of 2008.
Gross margin percentage in the third quarter of 2009 was 51.6% compared to 56.3%
in the third quarter of 2008. Gross margin percentage was significantly impacted
by volume and, to a lesser extent, a moderate decline in average transaction
pricing. We experienced an increase in awards of new and expanded exclusive or
near-exclusive long-term enterprise relationships with large pharmaceutical
companies during the latter portion of fiscal 2008 and also continuing into
2009, including several with whom we had very little business in the past. In
exchange for these long-term enterprise relationships with large pharmaceutical
companies, which are targeted to generate larger volumes of business, we have
made selective pricing concessions which has lowered averge transaction pricing
and we believe will have the effect of lowering overall average transaction
pricing in the future as more studies performed under these agreements become
active and generate revenue. The negative impacts of volume on the gross margin
percentage compared to the prior year's quarter was partially offset by the
elimination of legacy costs associated with processing the CCSS backlog during
the period we integrated the CCSS operations and lower depreciation and
amortization.
Operating income for the third quarter of 2009 was $4.7 million or 20.7% of
total net revenues compared to $10.6 million or 31.1% of total net revenues in
the third quarter of 2008. Total expenses were $18.0 million in the third
quarter of 2009, a decrease of $5.4 million from $23.4 million in the third
quarter of 2008. Overall expenses decreased primarily to the elimination of
transition costs related to the integration of the CCSS operations which were
completed in September 2008. We also experienced lower bonus expense in 2009
consistent with our reduced operating results and lower depreciation as some of
our EDC equipment is fully depreciated and the amortization of CCSS intangibles
is declining. Our effective income tax rate for the third quarter of 2009 was
39.1% compared to 35.8% in the third quarter of 2008.
Net income for the third quarter of 2009 was $2.8 million, or $0.06 per diluted
share, compared to $6.9 million, or $0.13 per diluted share in the third quarter
of 2008.
Commencing in the fourth quarter of 2008, general business and economic
conditions have deteriorated globally. Starting in the fourth quarter of 2008,
we experienced an increased focus in our routine (Phase I - IV) business, a
decline in the number of Thorough QTc bookings, and a delay in starts for
certain Thorough QTc trials, and these trends have continued through fiscal
2009. We recorded a book to bill ratio of 1.9 in the third quarter ended
September 30, 2009 due to a strong increase in routine bookings, which increased
23% sequentially and 15% compared to the third quarter a year ago. We believe
the increase in routine business will provide us with a base of business into
the future; however, this business will take longer to turn into revenue. We
believe that the delays in Thorough QTc trials are related to timing as the
result of the uncertain economic environment, especially in small to midsize
customers. Sponsors may delay the running of Thorough QT trials until later in
the drug development cycle, though regulatory guidance ultimately requires that
they be performed.
We have recently implemented certain cost reductions. Our operations structure
includes a high percentage of fixed costs. Higher future transaction volumes,
should they occur, may offset the impact on our gross margin percentage of any
price reduction. Overall, we believe the fundamental drivers of our core
business remain positive. However, a continued weakened global economy could
have a negative impact on future results of operations.
The following table presents certain financial data as a percentage of total net revenues:
Three Months Ended September 30, Nine Months Ended September 30,
2008 2009 2008 2009
Net revenues:
EDC licenses and services 4.6 % 0.0 % 4.2 % 3.5 %
Services 71.3 % 70.3 % 73.3 % 68.4 %
Site support 24.1 % 29.7 % 22.5 % 28.1 %
Total net revenues 100.0 % 100.0 % 100.0 % 100.0 %
Costs of revenues:
Cost of EDC licenses and services 1.3 % 0.0 % 1.3 % 1.2 %
Cost of services 28.5 % 33.4 % 29.3 % 32.5 %
Cost of site support 13.9 % 15.0 % 14.1 % 14.9 %
Total costs of revenues 43.7 % 48.4 % 44.7 % 48.6 %
Gross margin 56.3 % 51.6 % 55.3 % 51.4 %
Operating expenses:
Selling and marketing 9.2 % 13.4 % 10.0 % 13.8 %
General and administrative 12.5 % 13.1 % 13.3 % 15.0 %
Research and development 3.5 % 4.4 % 3.1 % 4.4 %
Total operating expenses 25.2 % 30.9 % 26.4 % 33.2 %
Operating income 31.1 % 20.7 % 28.9 % 18.2 %
Other income (expense), net 0.7 % -0.3 % 0.9 % -0.5 %
Income before income taxes 31.8 % 20.4 % 29.8 % 17.7 %
Income tax provision 11.4 % 8.0 % 11.0 % 7.2 %
Net income 20.4 % 12.4 % 18.8 % 10.5 %
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Three Months Ended September 30, 2008 Compared to Three Months Ended
September 30, 2009.
The following table presents our consolidated statements of operations with
product line detail (dollars in thousands):
Three Months Ended September 30,
2008 2009 Increase (Decrease)
EDC licenses and services:
Net revenues $ 1,564 $ - $ (1,564 ) (100.0 %)
Costs of revenues 456 - (456 ) (100.0 %)
Gross margin $ 1,108 $ - $ (1,108 ) (100.0 %)
Services:
Net revenues $ 24,184 $ 15,969 $ (8,215 ) (34.0 %)
Costs of revenues 9,674 7,577 (2,097 ) (21.7 %)
Gross margin $ 14,510 $ 8,392 $ (6,118 ) (42.2 %)
Site support:
Net revenues $ 8,182 $ 6,757 $ (1,425 ) (17.4 %)
Costs of revenues 4,698 3,418 (1,280 ) (27.2 %)
Gross margin $ 3,484 $ 3,339 $ (145 ) (4.2 %)
Total
Net revenues $ 33,930 $ 22,726 $ (11,204 ) (33.0 %)
Costs of revenues 14,828 10,995 (3,833 ) (25.8 %)
Gross margin 19,102 11,731 (7,371 ) (38.6 %)
Operating expenses:
Selling and marketing 3,126 3,056 (70 ) (2.2 %)
General and administrative 4,254 2,977 (1,277 ) (30.0 %)
Research and development 1,173 989 (184 ) (15.7 %)
Total operating expenses 8,553 7,022 (1,531 ) (17.9 %)
Operating income 10,549 4,709 (5,840 ) (55.4 %)
Other income (expense), net 251 (82 ) (333 ) (132.7 %)
Income before income taxes 10,800 4,627 (6,173 ) (57.2 %)
Income tax provision 3,870 1,808 (2,062 ) (53.3 %)
Net income $ 6,930 $ 2,819 $ (4,111 ) (59.3 %)
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The following table presents costs of revenues as a percentage of related net revenues and operating expenses as a percentage of total net revenues:
Three Months Ended September 30, Increase
2008 2009 (Decrease)
Cost of EDC licenses and services 29.2 % N/A N/A
Cost of services 40.0 % 47.4 % 7.4 %
Cost of site support 57.4 % 50.6 % (6.8 %)
Total costs of revenues 43.7 % 48.4 % 4.7 %
Operating expenses:
Selling and marketing 9.2 % 13.4 % 4.2 %
General and administrative 12.5 % 13.1 % 0.6 %
Research and development 3.5 % 4.4 % 0.9 %
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EDC
On June 23, 2009, we completed the sale of certain assets relating to our EDC
operations. Under the terms of the transaction, OmniComm Systems, Inc. issued
8.1 million shares of common stock and assumed certain liabilities including
deferred revenue relating to our EDC operations in exchange for our EDC assets
which primarily included our EDC software, applications and fixed assets and
$1.15 million in cash we paid.
Revenues
The decrease in services revenues was primarily due to a $6.7 million reduction
in transaction revenue related to lower volume of transactions performed in the
three months ended September 30, 2009 as compared to the three months ended
September 30, 2008. There was also a decrease in average revenue per transaction
that was largely due to certain lower transaction prices which resulted in a
decrease in revenue of approximately $0.8 million. Project management fees,
excluding reporting configuration revenue, decreased $0.5 million, consistent
with the decreased Cardiac Safety activity. The balance of the decrease of
$0.2 million is comprised of a number of smaller items.
Site support revenues decreased primarily due to $0.4 million of one-time
billing in the quarter ended September 30, 2008 on units rented in prior periods
and to a reduction in equipment sales of $0.4 million. The balance of the
decrease is comprised of a number of smaller items totaling $0.6 million,
including a decrease in average rental rates and other one-time adjustments in
2008.
Costs of Revenues
The decrease in the cost of services was primarily due to $1.4 million of costs
recognized in the third quarter of 2008 associated with the CCSS operations. We
completed the integration of the CCSS acquisition in the third quarter of 2008
with the complete transfer of all operating activities from the CCSS Reno
facility into our operations in Philadelphia and Peterborough. Additionally,
variable incentive compensation expense decreased $0.4 million due to reduced
accruals based on operating results. Labor costs decreased $0.3 million as a
result of efficiency initiatives realized in 2009. There was also a $0.2 million
decrease in telephone and connectivity expenses due to lower rates in 2009. A
$0.1 million increase in depreciation due to systems placed in service in 2009
and $0.1 million of other increases in expense partially offset these decreases.
The increase in the cost of services as a percentage of service revenues
reflects the fact that some of the costs do not necessarily change in direct
relation with changes in revenue.
The decrease in the cost of site support, both in absolute terms and as a
percentage of site support revenues, was primarily due to a $0.7 million
decrease in depreciation expense as older, more expensive ECG equipment has
become fully depreciated and a $0.3 million decrease in freight. Additional
smaller decreases totaling $0.3 million occurred in costs of equipment sold,
labor and other expenses.
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