Our Toronto facility covers all phases of drug product development from early-phase formulation development to clinical trial material to commercial supply in the same plant using scalable equipment for non-GMP and GMP Work. Our experts at the Toronto facility are ready to address your needs for highly potent, low potent, complex formulations, pediatric dosage forms, patent-extension strategies, as well as conventional oral solid formulations.
Unique Offerings & Specialized Capabilities:
This site features a strong regulatory inspection history from all major international regulatory agencies.
Learn more about the specific equipment and capabilities at this site by downloading our Site Fact Sheet.