Reaching market safely and efficiently

Exova helps your products to reach markets quickly and safely by supporting you with timely and rigorous testing of your process validation and production batches.

Our experts carry out full specification testing such as HPLC assay, residual solvents, and dissolution, including physical tests: hardness, disintegration, and friability. Microbiological services include bacterial endotoxin, pathogens, and sterility/PET. Exova laboratories are GMP compliant and have the capabilities to meet your batch release testing requirements.

Pharma batch release testing

Exova’s capabilities in Pharmaceutical batch release testing include:

  • Disintegration
  • Dissolution
  • Hardness
  • Friability
  • Particle size (HIAC)
  • Dimensional analysis
  • Elemental Impurities by USP <233> using ICP-MS
  • HPLC with RI, UV, fluorescence, conductivity and PDA detectors
  • Headspace Gas Chromatography
  • Ion Chromatography
  • Gas Chromatography - Mass Spectrometry
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Pharmaceutical testing facilities

2395 Speakman Dr.,
Mississauga, ON L5K 1B3

Contact: Larissa Hillar - Operations Manager
Tel: +1 905 822 4111

Fax: +1 905 823 1446

Email: americas@exova.com

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9240 Santa Fe Springs Road,
Santa Fe Springs, CA 90670

Contact: Eric Lindsay - General Manager
Tel: +1 562 948 2225

Fax: +1 562 948 5850

Email: americas@exova.com

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Plot 598-221, Dubai Investments Park 1, The Green Community, P.O. Box: 34924,
Dubai

Contact: Jason Dodds - Managing Director
Tel: +971 4 885 1001

Fax: +971 4 885 4004

Email: middle.east@exova.com

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