Introduction to Pharmaceutical Auditing Techniques Workshop
Introduction to Pharmaceutical Auditing Techniques
September 1, 2021 | 9:00 am – 5:00 pm
Auditing of contractors, vendors, and suppliers in the Pharmaceutical industry is not only a regulatory requirement but also a critical Quality practice. Companies are outsourcing more and more of their capabilities to outside experts but the importance of establishing the GMP compliance and Quality systems status of these parties has been undervalued. Many companies fail to appreciate that all their contractors, vendors and suppliers are an extension of their own company and must therefore be held to the same standard that’s expected of them.
Data integrity is a key component in making informed decisions within any regulated organization. Reliable data promotes good decisions. Unmanaged and inaccurate data
The analytical testing requirement under Cannabis Regulations involves understanding various tests including wet chemistry, chromatography and microbiology, which will be introduced, discussed in-depth and interpreted.
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