Diteba is a cGMP/GLP pharmaceutical laboratory located near Toronto, Canada that offers analytical R&D services including method development and validation, bioanalytical testing, quality control release testing, stability testing, and in vitro release testing. The company has over 10,000 square feet of laboratory space equipped with state-of-the-art instrumentation. Diteba's team of senior scientists have extensive experience across various therapeutic areas and analytical techniques.
11. Regulatory History DATE REGULATORY AGENCY CATEGORY RATING/Status Sep 2005 Health Canada Pharmaceuticals C (Compliant) July 2006 Health Canada Control Drugs and Substances Status: licensed Feb 2008 Health Canada Biologicals; Pharmaceuticals C (Compliant) Feb 2009 Health Canada Class A Precursors Status: licensed Mar 2010 Health Canada Biologicals; Pharmaceuticals C (Compliant)
Diteba has a dedicated Stability and Analysis group providing services for all stages of drug development, from early research & development to commercial/post approval studies, in full compliance with ICH, Health Canada, EMEA and FDA requirements. Our Stability department is integrated within the laboratory complex and provides the following services for all storage conditions. Every chamber is electronically monitored and on automated generator back-up.