This webinar will deal with the usage of the FDA, GAMP, 21 CFR Half 11, “Digital Data” / “Electronic Signatures”, and other relevant trade software validation fashions, coupled with the ISO 14971 / ICH Q9 Product Risk Management fashions, to construction, run, and doc acceptable software validations. The FDA and other regulatory agencies have acknowledged that software validation can realistically only be completed effectively if “danger-based mostly”.A How can this are achieved within the “actual world”. This webinar will deal with software that’s:
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Logging onto the Lawsense website, customers can select the doc they require at any time they choose and instantly start to finish it. The ‘try before you … Read More