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The company's consistent growth over this period has been due to
its ability to expand its services offering to meet the needs of STATKING's target
market, emerging and mid-size pharmaceutical and medical device companies. The addition
of clinical trial management services, clinical study monitoring services, medical
coding software, electronic data capture services, medical writing, medical monitoring and safety reporting
services all provided solutions to problems and accelerated development timelines
of STATKING's client companies.
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Today, the company employs a staff of product development specialists
that are heavily involved in all phases of the Client's development program including
protocol development and study management tasks. STATKING's highly experienced team
of professionals has been instrumental in achieving regulatory approval for a number
of new medical devices, drugs and biologics. At STATKING, our team is committed
to providing services that meet or exceed all Federal Guidelines and Regulations
for Good Clinical Practice.
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