This webinar will provide a clear understanding of the basics of GLP and cGMP compliance in drug development (non-clinical testing, and manufacturing of drugs).
Get a comprehensive overview of the key compliance regulations required for GLP laboratory compliance for non-clinical testing in drug development. And, also a comprehensive overview of the cGMP regulations for the manufacturing in pharmaceutical development.
No FUDs are expected. Compliance based on the regulations are well established, and documented in key guidance documents. Any personnel working in these areas must adhere to the regulations. It is “black and white”, and straightforward.
Visit bit.ly/2fdp4Du for more info and registration.