WEBINAR: FDA's 21 CFR Part 11 Add-on Inspections: Address Software That is Supporting the Company's Quality System and CGMP Documentation

Market opportunities arise in providing solutions for cGMP software verification and validation, addressing increased FDA scrutiny. Demand exists for expertise in FDA guidelines, risk management ...

Batch Record Review and Product Release Training Webinar: FDA 21 CFR 210/211 Expectations, Deviation Handling, CMO Oversight, and ICH Q10–ISO 13485 Alignment (ONLINE EVENT)

The main market opportunity lies in providing practical, inspection-ready training for batch record review tailored to pharma, biologics, and medical device fields. By focusing on real-world ...
Mena FN

WEBINAR: FDA's 21 CFR Part 11 Add-On Inspections: Address Software That Is Supporting The Company's Quality System And CGMP Documentation

(MENAFN- GlobeNewsWire - Nasdaq) Market opportunities arise in providing solutions for cGMP software verification and validation, addressing increased FDA scrutiny. Demand exists for expertise in FDA ...