Analytical testing and quality control ensure product performance and regulatory compliance.

Analytical development services and quality control testing support all phases of product and process development from raw materials to commercial batch release and are key to the success of the final product.

Exova SL Pharma’s analytical development and quality control testing services include:

  • Raw material testing
  • USP/EP compendial testing
  • Commercial release and stability testing
  • Forced degradation studies
  • ICH methods development and validation
  • ICH stability testing and storage for drug substances and finished products
  • Development and validation of dissolution methods
  • Development and validation of methods for cleaning
  • Analytical support for all stages of CMC development
  • Analytical trouble-shooting
  • Technology transfer

At Exova SL Pharma we work with both large companies and start-up organizations. Our team of highly experienced scientists work closely with you to guide you through all aspects of analytical development, ensuring an efficient and collaborative support on time and within budget.

Pharmaceutical testing facilities

2395 Speakman Dr.,
Mississauga, ON L5K 1B3

Contact: Larissa Hillar - Operations Manager
Tel: +1 905 822 4111 (ext. 10614)

Fax: +1 905 823 1446

Email: americas@exova.com

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1300 First State Blvd, Suite C,
Wilmington, DE 19804

Contact: Waheed Sheikh - President
Tel: +1 302-636-0202

Fax: +1 302-636-0204

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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