Our Virtual Quality Managementâ„¢ product is specifically designed to help pharmaceutical companies comply with regulatory requirements. A dedicated quality professional works directly for you on a part-time basis to provide a cost-effective solution.
Amongst the tasks carried out by this quality assurance specialist are:
- Setting up quality systems and standard operating procedures
- Auditing CROs and investigational medicinal product manufacturers for compliance with GCP and GMP
- Releasing supplies
- Drawing up technical agreements with each contractor
- Good manufacturing practice documentation reviews
- Ongoing project reviews and problem solving