What are the Current Good Manufacturing Practice regulations (cGMP) for Finished Pharmaceuticals (cGMP)? Why is it required to follow these regulations? This seminar will provide a review of cGMP ...
Lapse spotlights wider actions to ensure data accuracy. Key to maintaining public confidence in the safety and efficacy of medical products-particularly innovative cellular and gene therapies-is for ...
Agency guidance and industry standards aim to reduce lapses and improve quality operations. FDA has long emphasized the importance of reliable and accurate data in ensuring drug safety, quality, and ...
This training unlocks opportunities for companies to modernize GxP validation by shifting to Computer Software Assurance, ensuring data integrity and compliance with FDA regulations, and addressing ...
FDA demands accurate manufacturing and test information to ensure product quality. It may seem to some members of the biopharmaceutical manufacturing community that incomplete records and faulty ...
Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "Data Process Mapping Tools and Strategies in Data Integrity Governance (Sept 5, 2025)" training has been added to ResearchAndMarkets.com's offering. This ...
The agency proposes significant revisions to oversight programs for drugs and medical products. As part of agency initiatives to strengthen its oversight of human food and food products, FDA is ...
Data integrity is a major concern in the regulated pharmaceutical industry due to discovery of either poor record management practices or falsification of data. This has resulted in numerous FDA ...
Dublin, July 15, 2025 (GLOBE NEWSWIRE) -- The "CSV Masterclass - 2025 (3-Day Boot Camp)" training has been added to ResearchAndMarkets.com's offering. This seminar is intended for those involved in ...
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