Our Quality Assurance (QA) group are dedicated to ensuring we consistently achieve the highest standards of quality management across documentation and records, materials management, laboratory controls and cGMP.
They are here to support and work with you at every stage of the process, managing GMP issues and audits, and supporting any range of validation effort, including process, methods and cleaning validations.
You can be confident that our facilities operate to full cGMP and that our SOP systems are comprehensive, reaching every aspect of material flow.
Our SOPs govern:
- Material arrival
- Generation of Master Production Records
- Generation of specifications
- Cleaning validation/verification
- Packaging and shipping of API