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Line 3: In the past years, the application of GDocP is also expanding to cosmetic industry, excipient and ingredient manufacturers. == ~~GDP /~~ GDocP standards == === Documentation creation === * Contemporaneous with the event they describe<ref name=EUGMP4 />{{Rp\|___location=¶4.8}}<ref name="FDAGCP">{{HHS content\|source={{Cite web \|date=April 1999 \|title=Guidance for Industry - COMPUTERIZED SYSTEMS USED IN CLINICAL TRIALS \|url=https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/fda-bioresearch-monitoring-information/guidance-industry-computerized-systems-used-clinical-trials \|url-status=live \|archive-url=https://web.archive.org/web/20200924221420/https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/fda-bioresearch-monitoring-information/guidance-industry-computerized-systems-used-clinical-trials \|archive-date=24 September 2020 \|access-date=15 October 2022 \|website=U.S. Food and Drug Administration}}}}</ref><ref name=WHO4 /><ref name=ICH7 />

Good documentation practice: Difference between revisions