Pharmaceutical Analytical Consultancy expertise, with over 20 years global experience meeting pharmaceutical regulatory requirements, applied to product development and Quality Assurance (QA) programs.
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
- Data envelopment analysis (DEA) Sample Handling/Systems
- Clean Room Assessment and Monitoring
- On-Site Good Manufacturing Practice (GMP) / Good Laboratory Practice (GLP) Training
- Quality Management Systems
- Regulatory Affairs
- Supplier Qualification & On-Site GMP Audits
- Validation Support (Development, Planning, Equipment)
Pharmaceutical News & Events
- Watch our RDD2024 Workshop on Generic Nasal Suspensions
- Determination of Particles in Pharmaceuticals - Article
- Discover our Audit Live Tool for direct access to our scheduled audits
- Extractables/Leachables Lab Tour - Request access
- Medical Device Extractables & Leachables Studies
- Glycosylation Analytical Approaches for Antibody Therapeutics
- Rapid Determination of Low/Trace Level Benzene in Pharmaceutical Excipients and Finished Products
- mRNA Analytics: Capping Efficiency, Sequencing, Poly-A Tail, dsRNA
Intertek Pharmaceutical Services
P.O. Box 470
291 Route 22 East
Salem Industrial Park
Whitehouse, NJ 08888
USA
Sample Size and Pricing Guide (PDF)
Download our Pharmaceutical Testing brochure (PDF)
Download our Intertek Pharmaceutical Services Brochure
Download our Custom Extractables and Leachables Solutions Brochure
Pharmaceutical Services
