Post-Approval Consultation:

  PDi will provide regulatory compliance advice in preparing and reviewing sales and marketing aids and label changes.
PDi can arrange coordination of post-marketing surveillance requirements including collection, processing, tracking and reporting of adverse events.
PDi offers advice when planning for new indications, presentations or process changes.

 


a. Canadian Strategic Planning & Agency Representation
b. Preclinical & Clinical Development
c. Submission Development & Support
d. Post-Approval Consultation