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Good manufacturing practices inspection policy for drug establishments (POL-0011)

https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/good-manufacturing-practices/policies-standards/inspection-policy-canadian-drug-establishments.html

Apr 3, 2019 .... Canadians rely on drugs produced from both domestic and foreign manufacturers through complex global supply chains involving both raw materials and finished dosage forms. A high percentage of health products are imported into Canada, with many products containing ingredients from other countries. To facilitate uniform application of these requirements and help

Class 3, non-in vitro diagnostic devices (nIVD), new and amendment applications

https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/international-medical-device-regulators-forum/class-3-non-vitro-devices-new-amendment-applications.html

Jun 18, 2019 ... For further information on how to complete the Health Canada Medical Device Licence form consult our Guidance Document - How to Complete the Application for a New Medical Device Licence. Classification New and amendment applications: Required 1.06 - Quality Management System, Full Quality System or Other Regulatory Certificates Folder name: 1.06-QMS Full QS or Other

Class 4, non-in vitro diagnostic devices (nIVD), new and amendment applications

https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/international-medical-device-regulators-forum/class-4-non-in-vitro-devices-new-amendment-applications.html

Jun 18, 2019 ... Device Licence form consult our Guidance Document - How to Complete the Application for a New Medical Device Licence. Classification New and amendment applications: Required 1.06 - Quality Management System, Full Quality System or Other Regulatory Certificates Folder name: 1.06-QMS Full QS or Other Regulatory Certs IMDRF Health Canada content This subsection

European Union (EU) - Export requirements for fish and seafood - Canadian Food Inspection Agency

http://www.inspection.gc.ca/food/exporting-food/requirements-library/european-union-fish-and-seafood/eng/1304221213916/1304221299574

Jun 20, 2019 ... requirements Other information Eligible/Ineligible product Eligible All fish and seafood products Pre-export approvals by competent authority of importing country Establishments Establishments must appear on the appropriate establishment list administered by Directorate-General for Health and Food Safety (DG-SANTE). The four (4) lists pertinent to fish and seafood

Excise and GST/HST News - No. 104

https://www.canada.ca/en/revenue-agency/services/forms-publications/publications/news104/news104-excise-gst-hst-news-no-104-june-2018.html

Nov 6, 2018 ... federal excise duty on most legally available cannabis products, effective when non-medical cannabis becomes legally available for retail sale. The cannabis excise duty will generally not apply to packaged cannabis products that contain 0.3% or less tetrahydrocannabinol (THC) or to Health Canada approved pharmaceutical products with a Drug Identification Number

European Union (EU) - Export requirements for fish and seafood - Canadian Food Inspection Agency

https://www.inspection.gc.ca/food/exporting-food/requirements-library/european-union-fish-and-seafood/eng/1304221213916/1304221299574

Jun 20, 2019 ... requirements Other information Eligible/Ineligible product Eligible All fish and seafood products Pre-export approvals by competent authority of importing country Establishments Establishments must appear on the appropriate establishment list administered by Directorate-General for Health and Food Safety (DG-SANTE). The four (4) lists pertinent to fish and seafood

Exporting food: A step-by-step guide - Canadian Food Inspection Agency

https://www.inspection.gc.ca/food/exporting-food/a-step-by-step-guide/eng/1503509841003/1503509896626

Jun 14, 2019 ... could jeopardize the entire Canadian food industry. Exception: If you export food solely under the Food and Drug Regulations, you might not have a CFIA registration or licence number at this time. Preventive control plan (PCP) The preventive control plan (PCP) is a written document that demonstrates how hazards and risks to food commodities are controlled. You

Fees in Respect of Drugs and Medical Devices Regulations

https://laws.justice.gc.ca/eng/regulations/SOR-2011-79/page-1.html

Jun 3, 2019 ...) The purpose of these Regulations is also to remit, in whole or in part, certain of those fees. Application Marginal note:Non-application 3 These Regulations do not apply in respect of (a) a drug that is for veterinary use only; (b) a drug that is a natural health product; (c) a drug that is the subject of an extraordinary use new drug submission filed under section C

Former – Labelling requirements for meat and poultry products - Food - Canadian Food Inspection Agency

http://www.inspection.gc.ca/food/requirements-and-guidance/labelling/-f-for-industry/-f-meat-and-poultry-products/eng/1515522793732/1515522794717?chap=0

Jul 22, 2019 ...Former – Labelling requirements for meat and poultry products Important notice On December 14, 2016, amendments to nutrition labelling, list of ingredients and food colour requirements of the Food and Drug Regulations came into force. Regulated parties have a five (5) year transition period to meet the new labelling requirements. This former page

Risk management approach for chlorhexidine and its salts

https://www.canada.ca/en/environment-climate-change/services/evaluating-existing-substances/risk-management-approach-chlorhexidine-salts.html

Jun 28, 2019 ...]. Health Canada. [modified 2017-4-26]. Establishment Licences. Ottawa (ON): Health Canada. [accessed April 5, 2016]. Health Canada. 2018. Good manufacturing practices guide for drug products (GUI-0001) [PDF]. Ottawa (ON): Government of Canada. [ISEDC] Innovation, Science and Economic Development Canada. 2015. Pharmaceutical Industry Profile. [accessed January 22

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