Pharmaceutical Analytical and QA Consulting
Our global expertise in regulatory requirements, coupled with our reputation for technical knowledge accrued over many years, enables Intertek to provide a range of consulting services for analytical research and QA in the pharmaceutical industry.
Intertek’s pharmaceutical consulting services can be contracted independently, or in conjunction with scientific projects. Typically consulting programs are designed to meet specific client requirements and can range from small to large in scope. In addition, services can be provided in-house, on site at multiple client locations or at third party facilities.
Analytical Research & Development (cGMP)
- Complete Analytical Program Design
- Laboratory Design & Instrumentation
- Validation Planning & Design
Quality Assurance
- DEA Sample Handling/Systems
- Clean Room Assessment and Monitoring
- On-Site GMP/GLP Training
- Quality Management Systems
- Regulatory Affairs
- Supplier Qualification & On-Site GMP Audits
- Validation Support (Development, Planning, Equipment)
Request more information to see how Intertek can help your organization with Pharmaceutical Analytical and QA Consulting.