Measuring and Documenting Quality, Risks and Failures in GMP
University of Birmingham, Edgbaston, Birmingham
10 - 11 June 2025
£995 per attendee
Learn how quality, risks, and failures are measured and documented in GMP medicines manufacturing.
Over this two-day course you will 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 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 (Corrective and Preventive Action) to prevent issues from happening again.
Who should attend:
This course Is suitable for
Those developing careers in Quality Control, Quality Assurance, and Manufacturing in the Pharmaceuticals industry;
Scientists looking to broaden their knowledge of good manufacturing processes; and
Graduates looking to prepare themselves for entering the advanced therapy and medicinal product industry.
To register:
E-mail Resilience-skills at the University of Birmingham.