Pharmaceutical Analytical and QA Consulting

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)