The traceability of data provided by the Quality control lab within the pharmaceutical industry is a critical chain for the safe release of products. As a result, looking at ways to improve data integrity continues to be a topic of discussion. There are many areas of pharmaceutical manufacturing that require documentation. We often see companies continue to rely on humans for data transcription.
Presented on December 5th and now available on demand, this webinar addresses specific challenges associated with microbiology and related documentation. Please attend to see how current technologies and digitalized solutions help smooth over those hurdles. In this short webinar, we will review changes made to Equipment Qualification, Compressed Gas Sampling, and Sterility Testing to help you gain confidence with the information being acquired and documented.
