Cyton’s Quality Assurance (QA) team can support clients in setting up or maintaining a Quality Management System (QMS) with Standard Operating Procedures (SOPs) defining how work tasks are carried out. Cyton can help ensure you have fully controlled procedures, maintaining records of document versions, change history and scheduling regular system reviews. The QA team has extensive experience in auditing SOP systems. The team can help your company rationalise your systems and identify unnecessary duplication of activity, providing added value to our audit process.
Cyton’s QA team has experience in performing GMP audits for the manufacturers of Finished Products and Active Pharmaceutical Ingredients (APIs) and distribution plants worldwide.
Our specialist services in QA and GMP include the following:
Quality Assurance Services
- Development and Maintenance of QA Systems
Creation of controlled bespoke Quality Assurance Systems.
- Creation and Implementation of SOPs
Improvement of existing standard operating procedures (SOPs) or generation of SOPs. Implementation and training phases of these SOPs.
- SOP and QA System Audits
Quality Assurance System auditing, corrective action plans and implementation of improvements.
- cGMP Advice and Support
Up to date knowledge and understanding of Good Manufacturing Practice (GMP) requirements.
- GMP Auditing
GMP auditing of Finished Product and Active Pharmaceutical Ingredient manufacturing facilities.
- Quality system review
Review of quality systems and procedures for compliance with EU GMP requirements
Whether you have need of long-term quality management support or a one-off audit, Cyton can offer a valuable external view and help you optimise your procedures for maximum efficiency.