SeerPharma was invited by the Stevanato Group and Lonza to present on Pharmaceutical Quality Management System (QMS) Certification at The Innovative Solutions for Pharmaceutical Packaging Roadshow in Singapore.
The workshop focused on the process of developing biopharmaceuticals, highlighting different points of view from container manufacturing, drug development, through to process transfer and industrialisation.
The presentation from SeerPharma addressed how to design and develop a Pharmaceutical QMS. Leaning on our 30 years of experience in industry, SeerPharma presented best practices in:
- How to best plan for implementing a Quality System
- Ideal document hierarchy to use
- The responsibility of Management
- How to integrate elements of the Quality System
- And the importance of how language should be used for procedures and defining Quality System elements
By addressing these elements early on, in the Design and Development of a Quality Management System, Pharmaceutical organisations can achieve greater confidence in being compliant and achieving their Quality Assurance objectives.
Contact us if you need assistance with the design and development of a Pharmaceutical Quality System, or if you’d like assistance in getting the most out of your current QMS?
This post comes from our April 2018 Journal. You may also be interested in:
