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Standards / Methodologies:

Bioanaltyical method development and validation services are conducted in compliance with the United States Food & Drug Administration (FDA), Guidance for Industry Bioanalytical Method Validation (21 CFR Part 58) and in accordance with Custom Biologics'T Standard Operating Procedures. Pharmaceutical testing, bio-analytical method validation and data analysis are conducted under GLP regulations according to FDA guidelines (21 CFR Part 58), 21 CFR Parts 11 and 58 Compliant

Contact

416.479.3773 Ext: 101

 Company Website

115 Skyway Ave

Toronto, ON M9W 4Z4 CA

DISCLAIMER: This Laboratory Profile was provided by the company above.