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Home > Drugs & Health Products > Drug Products > Applications & Submissions > Forms

Forms

arrow ADR Expedited Reporting Summary for ADRs Occuring During Clinical Trials
Date: 2003-03-31
arrow Animal Tissue: Category IV
Date: 1996-02-06

arrow Animal Tissue: Labelling Standard
Date: 1995-02-06

arrow Authority to Sell Fee Reduction Request and Attestation Form
Date: 2003-05-01
arrow Certification: Submissions NDS, SNDS, NC
Date: 1995-06-05
arrow Category IV Drug Submission Certification
Date: 1997-05-05

arrow Certification: Changes in Manufacturer's Name and/or Product Name
Date: 2001-01-03

arrow Clinical Trial Site Information Form
Date: 2003-03-31

arrow Drug Establishment Licence : Fee Reduction Request
Date: 2003-09-01
arrow Drug Master File (DMF) Application Fee Form
Date: 2004-09-29
arrow Drug Product Ingredient Form
Date: 2004-10-20

Guidance and Questions and Answers for Drug Product Ingredient Form
Date: 2004-10-20
arrow Release of Revised Form IV and Form V, pertaining to the Patented Medicines (Notice of Compliance) Regulations
Date: 2006-10-13
 
Form IV: Patent List - Patented Medicines (Notice of Compliance) Regulations
Date: 2006-10-13
 
Form V: Declaration re: Patent List Patented Medicines (Notice of Compliance) Regulations
Date: 2006-10-13
arrow HC SC 3011: Drug Application for: Human, Veterinary, or Disinfectant Drugs and Clinical Trial Applications/Attestation
Date: 2002-08-02

arrow Labelling Standard and Category IV Submission Check List
Date: 2004-11-08
arrow Product Monograph Certification Form
Date: 2004-08-17

arrow Qualified Investigator Undertaking
Date: 2003-03-31

arrow Quaternary Ammonium Hard Surface Disinfectant/Sanitizer Products Certification
Date: 1997-03-21
arrow Research Ethics Board Attestation
Date: 2003-03-31
arrow Submission Certification: DIN
Date: 1995-04-13
arrow Submission Fee Application Form
Date: 2004-11-15
Last Updated: 2006-10-13 Top
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