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

Contact Intertek