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How a new investment is powering a revolution in clinical trial operations

pharmaphorum

In most cases, the EHRs and EDCs don’t communicate, so in order to share that data with trial organisers, staff members at medical centres must manually copy data between the EHR and an EDC. As an average Phase 3 trial amasses over 3.6

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Typical GMP documentation in a quality control laboratory

GMPSOP

Laboratory documents Records of testing include laboratory analyst note books, specific testing sheets, and analytical printouts, electronic records such as chromatographs, and ancillary records that support the compliance of the laboratory. Usually these sheets are linked to specific test methods.