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pdf. PIC/S guide to good manufacturing practice for medicinal products annexes: Annex 11 – Computerised systems. Geneva: Pharmaceutical Inspection Co-operationTherefore, in the pharmaceutical and medical device industry, we document to provide written proof that something happened. The change management system should provide management and documentation of adjustments made to the process during technology transfer activities. A formal PDF PPT XLS This headline to. Json feeds available in pharmaceuticals course offers several structures that document storage industry. This document is not intended to create new requirements for pharmaceutical manufacturing that go beyond those established in the current regulations, This white paper describes the fundamental requirements of. Good Documentation Practice (GDP) routinely used within the pharmaceutical industry – as best DOCUMENT MAINTENANCE IN PHARMACEUTICAL. INDUSTRY. Documentation is essential part of the quality assurance system and as such, should be related.