Are you a Patentee?

Filing

• Filing requirements and deadlines
• Forms
• Patentee's Guide to Reporting
• Online Filing of Form 2

The following documents will assist you in your filing:

• Top 10 checklist for filing Form 2
• CPI-adjustment factors
• Exchange rates
• DIP methodology
• Formulas for foreign price verification

Instructional videos

• Completing and submitting Form 1: Medicine Identification Sheet
• Acquisition of DIN(s) from a former patentee

Note that all filings should be sent to compliance@pmprb-cepmb.gc.ca

Scientific Review

• Human Drug Advisory Panel (HDAP) meeting schedule and filing requirements
• New format for electronic submission
• Human Drug Advisory Panel's terms of reference

Regulatory Affairs and Outreach Presentations and Webinars

• Complete list of presentations and webinars
• Topics of interest The list of topics of interest for patentees provides references to the outreach presentations, webinar presentations and NEWSletters

Frequently Asked Questions – Patentees

• Frequently asked questions – Patentees

Reporting Requirements

The main statutory reporting requirements are fully described in the following:

• Patented Medicines Regulations 
• Compendium of Policies, Guidelines and Procedures 
• Patentee's Guide to Reporting