GMP-Compliant Quality Assurance Systems

We provide a range of services to ensure that you and your contractors meet EU and FDA good manufacturing practice requirements.

These include:

• Preparation of standard operating procedures
• Preparation of validation master plans
• Preparation of site master files
• Staff training
• Dealing with regulatory authorities
• CAPA
• Technical/quality agreements

Our expertise covers active pharmaceutical ingredients, investigational medicinal products, sterile and non-sterile dosage forms and biotechnology products.