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Process improvements and in-person monitoring help U.S. pharmaceutical company achieve on time for Phase III clinical trials

Syner-G

pharmaceutical company to oversee a 6 month, DS manufacturing as Person-In- Plant (PIP) and assist with preparation of associated submission documents related to Phase III clinical trial batches. Download The Case Study The post Process improvements and in-person monitoring help U.S.

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How to develop GMP compliant software for quality management

GMPSOP

Fundamental requirements of GMP compliant software The critical objectives for developing a quality management software application are to make the quality concern investigations processes faster, more reliable, accurate, secure, and permanent for future reference. – Appropriate controls over systems documentation.