Quality Assurance and GMP Support

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.

GMP Services

  • 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.

Related pages

Manufacturing & Quality Projects

Cleaning validation

Analytical development and stability studies