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Licence, authorization and registration forms for drug and health products

https://www.canada.ca/en/health-canada/services/licences-authorizations-registrations-drug-health-products/licence-authorization-registration-forms-drug-health-products.html

Aug 24, 2016 ...Licence, authorization and registration forms for drug and health products Guidance documents for drug, medical device, natural health product and site licensing. Also find blood establishment, donor semen, cell, tissue and organ registration information. Services and information License an establishment or site for drugs or health products Guidance

Licences, authorizations and registrations for drug and health products

https://www.canada.ca/en/health-canada/services/licences-authorizations-registrations-drug-health-products.html

Dec 18, 2015 .... Drug and health product fees and submission requirements Information on complying with regulations, and drug submission fees and amendments. Licence, authorization and registration forms for drug and health products Guidance documents for drug, medical device, natural health product and site licensing. Also find blood establishment, donor semen, cell, tissue

Destruction of narcotics, controlled and restricted drugs and targeted substances by licensed dealers – Guidance document

https://www.canada.ca/en/health-canada/services/health-concerns/controlled-substances-precursor-chemicals/controlled-substances/compliance-monitoring/compliance-monitoring-controlled-substances/destruction.html

Sep 6, 2019 ... Loss or Theft Annex A: Definitions Annex B: Contact Information 1.0 Introduction The Controlled Drugs and Substances Act (CDSA) provides for the control of substances that can alter mental processes and that may produce harm to health and to society when diverted or misused. Except as authorized under its related regulations or via an exemption issued under

Requirements and process: Cannabis Licensing Application Guide

https://www.canada.ca/en/health-canada/services/drugs-medication/cannabis/industry-licensees-applicants/licensing-summary/guide.html

Aug 29, 2019 ... at each site. The address of each additional authorized site will appear on the licence, if it is issued. Intent to sell Indicate if there is intent to sell the product of the research (e.g., cannabis plants and/or cannabis plant seeds to a licensed cultivator, researcher, cannabis drug licence or exemption holder). Type of research Indicate the type(s

3.22 - Chapter 3 - Specific Registration Information by Feed Type - Animals - Canadian Food Inspection Agency

http://www.inspection.gc.ca/animals/feeds/regulatory-guidance/rg-1/chapter-3/eng/1329319549692/1329439126197?chap=22

Aug 13, 2019 ... and a feed will be approved as a drug. For the registration of veterinary biologics, a product licence is issued by the Terrestrial Animal Health Division of the CFIA, and an Establishment Licence Number must be shown on licensed veterinary biologics. A Drug Identification Number issued by HC must appear on any drug label. A Feed Registration Number must be indicated

Blood for transfusion or for use in the manufacture of a drug

https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/information-health-product/blood-donor.html

Jul 19, 2019 ...Blood for transfusion or for use in the manufacture of a drug On this page Who must register or be licensed How to apply for an authorization How to apply for registration How to apply for a blood establishment licence Requirement to report an error or accident Inspections The Blood Regulations Who must register or be licensed Blood establishments fall

Health products containing cannabis or for use with cannabis: Guidance for the Cannabis Act, the Food and Drugs Act, and related regulations

https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/applications-submissions/guidance-documents/guidance-cannabis-act-food-and-drugs-act-related-regulations/document.html

Jul 15, 2019 ... Introduction 1.1 Purpose 1.2 Background 1.3 Overview of New Legislative Framework 1.4 Scope and Application 2 Health Research and Clinical Trials with cannabis 2.1 Requirements for the authorization of a clinical trial 2.2 Research Licences under the Cannabis Act 3 Pre-market evaluation of health products under the FDA 3.1 Context 3.2 Prescription Drug Listing

Consulting with Canadians

https://www.canada.ca/en/government/system/consultations/consultingcanadians.html?departmentid=168&keywords=&lang=en&start=1&subjectid=0&submit=Apply&type=all&year=0

Sep 5, 2019 ... (GMP) prescribed in Part C, Division 2 of the Food and Drug Regulations (FDRs). The requirements of Division 2 apply to biologics, both as bulk process intermediates and in dosage form. This consultation document is based on a current version of PIC/S Annexes 2 and 14. The adoption of these current PIC/S documents will prepare Health Canada for the adoption

Consulting with Canadians

https://www.canada.ca/en/government/system/consultations/consultingcanadians.html?departmentid=0&lang=en&start=1&subjectid=0&type=all&year=0

Sep 5, 2019 ... Registration Decision PRD2019-09 Open - accepting input Health | Policy Aug 2, 2019 to Sept 16, 2019 2019-08-02 2019-09-16 Health Canada The Pest Management Regulatory Agency (PMRA) invites the public to submit written comments on the proposed registration decision for mefentrifluconazole and related end-use products. Proposed Registration Decision PRD2019-09

Publications listed by number - CRA

https://www.canada.ca/en/revenue-agency/services/forms-publications/publications.html

Aug 9, 2019 ... Duty Rates on Spirits and Wine Effective April 1, 2018 2018-02-15 EDBN24 Excise Duty Rates on Beer Effective April 1, 2018 2018-02-15 RC4476-NT Birth Registration and Canada Child Benefits - Northwest Territories 2018-03-16 NOTICE307 Cayoose Creek Indian Band Implements the First Nations Goods and Services Tax 2018-02-09 EDN47 New Form Y15D, Request for Formula

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