Preparation of finished product and active ingredient manufacturers and pharmaceutical wholesalers for regulatory inspections

Sto Solutions Ltd. provides consultations in connection with the preparation of manufacturers of active substances and finished medicinal products, including the conduct of a GAP-analysis and CAPA-plan and determination of the degree of readiness and compliance with the regulatory requirements for GMP. A similar service is provided for drug wholesalers as per GDP requirements.

GAP analysis is a performance evaluation method that determines whether certain requirements are met and, if not, what steps need to be taken to meet them. It is the basis for creating and constantly upgrading the quality management system.