Quality, risks, and failures are measured and documented in GMP medicines manufacturing. You'll learn how to apply Quality by Design, identify key quality and process factors, and set up strong Quality Management Systems to ensure safe, consistent products.

Topics covered include writing SOPs and electronic batch records, getting ready for audits and inspections, and keeping good documentation. The course also covers how to spot and manage risks, find the root causes of failures, and use CAPA to prevent issues from happening again.