Management Consulting - Acton, Massachusetts, United States
ACMP provides clinical, quality and regulatory consulting to medical device and pharmaceutical firms. Our principal consultant has over 15 years of experience in clinical operations and trial management including strategic clinical planning, clinical trial design, protocol development, data management, safety, quality assurance and regulatory (including FDA, and various European and Canadian agencies). ACMP also provides support with development and implementation of Standard Operating Procedures and day-to-day clinical trial management.
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