Health Canada
www.hc-sc.gc.ca
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Drugs and Health Products
Forms - Applications and Submissions - Biologics, Radiopharmaceuticals and Genetic Therapies
- Post-Notice of Compliance (NOC) Changes: Notices of Change (Level III) Form [2012-03-21]
- Drug Establishment Licence Application:Forms and Instructions (FRM-0033) [2011-04-01]
- Research Ethics Board Attestation [2003-03-31]
- ADR Expedited Reporting Summary for ADRs Occuring During Clinical Trials [2003-03-31]
- Clinical Trial Site Information Form [2003-03-31]
- Qualified Investigator Undertaking [2003-03-31]
- HC SC 3011: Drug Application for: Human, Veterinary, or Disinfectant Drugs and Clinical Trial Applications/Attestation [2010-10-26]
- Form V: Declaration Re: Patent List Patented Medicines (notice Of Compliance) Regulations - Second Person [2001-08-23]
- Certification: Changes in Manufacturer's Name and/or Product Name [2001-01-03]
- Submission Fee Application Form [2000-12-01]
- Form IV: Patent List - Pertaining To Patented Medicines Patented Medicines (notice Of Compliance) Regulations - First Person Application [2000-05-01]
- Category IV Drug Submission Certification [1997-05-05]
- Animal Tissue: Category IV [1996-02-06]
- Certification: Submissions NDS, SNDS, NC [1995-06-05]
- Submission Certification: DIN [1995-04-13]
- Animal Tissue: Labelling Standard [1995-02-06]
