Annex 22: Why AI Regulation In Pharma Manufacturing Matters More Than Ever

Annex 22 marks a paradigm shift in pharmaceutical manufacturing, not only because it closes the longstanding “AI grey zone” ...
News Medical

The critical role of data integrity in ensuring pharmaceutical quality

The pharmaceutical industry’s approach to data integrity has been historically manual, leveraging physical documentation and potentially unreliable paper-based ...
PharmTech

Why Pharma’s AI Agents Need Smaller, Domain-Specific Models First

Large-language models are excellent for general-use AI systems, but they don’t understand pharmaceutical companies’ ...
Forbes

Unlocking Growth And Ensuring Compliance: Data Management In Pharma

Amit Singh is a global leader specializing in transformative AI and Master Data Management solutions. Please reach out to him on LinkedIn. In the highly regulated pharmaceutical industry, companies ...
Business Wire

Efficient Batch Record Design and Review Course: Regulatory Requirements Applying to Batch Record Review, Pharmaceutical Documentation & the Quality System (ONLINE: November 11 ...

DUBLIN--(BUSINESS WIRE)--The "Efficient Batch Record Design and Review" training has been added to ResearchAndMarkets.com's offering. This online training is designed for professionals in the ...
Managingip.com

Supplementary experimental data acceptance criteria in pharmaceutical patent grant and confirmation procedures

Linlin Sun and Xia Zheng of AFD China Intellectual Property Law Office cite two key Chinese Supreme People’s Court cases to clarify the conditions under which supplementary experimental data is ...