Method validation and remediation

Exova can support your analytical research, validation, and investigation requirements. From the development of new, efficient analytical procedures through to method validation and remediation, our chemists will guide you through the processes to deliver and execute validated methods that meet regulatory demands and advance your laboratory testing programmes.

Pharma analytical method -development

We offer a full spectrum of methods including HPLC, UHPLC, LC-MS/MS, ICPMS, ICPOES, NMR, GC, and GCMS. We also conduct our analytical testing in accordance with ICH guidelines, keeping your business safe by ensuring you meet all regulatory demands.

Analytical method validation and development services include:

  • Stability indicating assays
  • Forced degradation studies
  • Process impurity method development and validation
  • Analytical standard characterisation
  • Extractables / leachables method development and validation
  • Pharmacokinetic, bioavailability, and bioequivalence method development and validation
  • Technical consulting
  • Cleaning validation method development and validation
  • Peak Identification
  • USP method verification
  • Column equivalency studies
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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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