Learn effective batch record review with our accredited training. Understand Master Batch Records, regulatory requirements, and best practices in pharmaceutical, biologic, and medical device ...

Regulatory Requirements Applying to Batch Record Review, Pharmaceutical Documentation & the Quality System Global regulations and expectations Regulations Update and Latest Developments in Industry ...

The FDA and its European counterpart, EMA, require drug manufacturers to have written procedures in place to document production and process controls, better known as batch records. Additionally, ...

Image Credit: Quality Stock Arts/Shutterstock.com. Batch vs. continuous manufacturing. For many years, the pharmaceutical industry was hesitant to incorporate continuous manufacturing into their ...

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 Pharmaceutical, Medical ...