Regulatory Filings

• Form 1: Medicine Identification Sheet (XLS)
• Form 2: Information on the Identity of Prices of the Medicine (Revised – Mandatory as of July 1, 2008)
  • Blocks 1, 2, 3, and Signature (XLS)
  • Block 4: Sales of the medicine by the reporting patentee in final dosage form in Canada (XLS)
  • Block 5: Publicly available ex-factory prices for Canada and other countries (XLS)
• Form 3: Revenues and Research and Development Expenditures Provided Pursuant to subsection 88(1) of the Patent Act (XLS)
• Notification of Intention to Sell

• Comparable Dosage Forms (PDF)
• Presentation on How to Report according to New Regulations (May 2008) (PPT)