Expertise in method development and validation, stability, trace organics, elemental impurities, and QC testing for more than 30 years
Intertek Pharmaceutical Services, located in Whitehouse, New Jersey, USA, is an outsourcing analytical services testing laboratory. FDA regulated, Good Manufacturing Practice (cGMP) compliant facility with DEA I-V availability. We specialize in:
- Pharmaceutical material testing
- Method development and validation
- Stability studies
- Extractable/Leachables
- Elemental impurities, analysis and trace metals
- Medical device testing
We provide complex and routine services to support the development of drug products, formulations, devices, and drug delivery systems for pharmaceutical and biotechnology companies. We also specialize in compound characterization, reference standard support, identification and quantitation of inorganic components, toxicology screening, product profiling, determining contaminants related to packaging materials and residue characterization.
Pharmaceutical Material Testing
Release testing of raw materials, excipients, APIs and finished pharma products
Analytical Method Development & Validation
Supports drug development across a range of analytical technologies
Elemental Analysis & Trace Metals
Supports pharmaceutical development and GMP production
Elemental Impurities
USP <232> and <233> elemental impurities testing
Extractables & Leachables & Medical Devices
Quantify and assess risk associated with potential leachable impurities
Stability Studies
Supports drug development, commercial stability studies, batch release and QC testing
Conferences & Trade Shows
Upcoming industry events and conferences
Pharmaceutical News & Events
- EVENT - Meet us at BIO-Europe Spring 2026 - Connect now.
- PRESS RELEASE: Expansion of capacity with acquisition of new facility in Melbourn, Cambridge
- PRESS RELEASE: Launch of extractables and leachables services for compliance with new Korean Pharmacopeia requirements
- PRESS RELEASE: Intertek partners with CrystecPharma to advance formulation science and accelerate development for dry powder inhalers
- NEW! Blog: Optimising Quality in Pharma Supply Chains
- 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
- Rapid Determination of Low/Trace Level Benzene in Pharmaceutical Excipients and Finished Products