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Applications for Medical Device Investigational Testing Authorizations Guidance Document

https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/investigational-testing-authorizations-guidance/guidance-document.html

May 2, 2019 .... In this case, the manufacturer of the device must sign the ITA application form, and regulatory correspondence is usually delegated to the drug sponsor. For Class III and IV devices, the pre-clinical information is submitted to Health Canada by the device manufacturer, and the study protocol and Informed Consent Forms (ICFs) are submitted by the sponsor of the drug

2015 Commissioner of Firearms report | Royal Canadian Mounted Police

http://www.rcmp-grc.gc.ca/en/2015-commissioner-firearms-report

Nov 12, 2019 ... refusals, 2011 to 2015 Year Refusals 2011 520 2012 670 2013 886 2014 805 2015 688 Total 3,569 Table 7: Reasons for firearms licence application refusals, 2015Footnote 5 Reason Refusals Court-ordered prohibition/probation 229 Domestic violence 40 Drug offences 25 Mental health 112 POL ineligibleFootnote 6 10 Potential risk to others 132 Potential risk to self 203

2016 Commissioner of Firearms report | Royal Canadian Mounted Police

http://www.rcmp-grc.gc.ca/en/firearms/2016-commissioner-firearms-report

Dec 3, 2019 ... 2,421 2013 2,497 2014 2,354 2015 2,347 2016 2,223 Total 11,842 Table 10: Reasons for firearms licence revocations, 2016 Footnote 5 Reason Revocations Court-ordered prohibition/probation 1,393 Domestic violence 66 Drug offences 20 Mental health 424 Potential risk to others 238 Potential risk to self 251 Provided false information 63 Unsafe firearm use and storage

Medical Devices Regulations

https://laws.justice.gc.ca/eng/regulations/SOR-98-282/FullText.html

Jun 17, 2019 ... Medical Devices Regulations SOR/98-282 FOOD AND DRUGS ACT Registration 1998-05-07 Medical Devices Regulations P.C. 1998-783 1998-05-07 His Excellency the Governor General in Council, on the recommendation of the Minister of Health, pursuant to subsections 3(3), 30(1) and 37(1)Footnote a of the Food and Drugs Act, hereby makes the annexed Medical Devices

Tobacco and Vaping Products Act

https://laws.justice.gc.ca/eng/acts/T-11.5/FullText.html

Nov 9, 2019 ... and the package containing it display, in the prescribed form and manner, the information required by the regulations about the product and its emissions, and about the health hazards and health effects arising from the use of the product and from its emissions. Marginal note:Information — packaging of tobacco products (1.1) No manufacturer shall package a tobacco product

Compliance and enforcement policy for health products (POL-0001)

https://www.canada.ca/en/health-canada/services/drugs-health-products/compliance-enforcement/good-manufacturing-practices/policies-standards/compliance-enforcement-policy-0001.html

May 7, 2019 ... under the Act has clearly defined responsibilities for the safety, efficacy and quality of health products imported or sold in Canada. Other parties may also be subject to the Act although they may not require an authorization from Health Canada to perform certain activities. For example, while wholesalers of non-prescription drugs and active pharmaceutical

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 ... Advertising/Marketing Agriculture Amendments Animals Children Communication Copyright/Trademarks/Patents Culture Development Economy Economic development Employment Environment Education Exporting/Importing Financial assistance and entitlements Food and drug Finance Foreign affairs Fisheries Government procurement Housing Heritage Human resources Health Immigration

Reporting Adverse Reactions to Marketed Health Products - Guidance Document for Industry

https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/reporting-adverse-reactions-marketed-health-products-guidance-industry/guidance-document.html

May 17, 2019 ... instruction document, may continue to send AR reports to MHPD by fax or by mail (see Appendix 4 for contact information). The preferred reporting format for AR reporting by MAHs via fax and mail is as follows: for drugs, the Council for International Organizations of Medical Sciences (CIOMS) Form IReference 13 for natural health products, the Mandatory Adverse

Narcotic Control Regulations

https://laws.justice.gc.ca/eng/regulations/C.R.C.,_c._1041/FullText.html

Jun 17, 2019 ... (benzoylmethylecgonine) or any of its salts, or any drug that is not in dosage form that contains such a substance, unless the cocaine, salt or drug is to be compounded by a pharmacist in accordance with or in anticipation of an authorization from a practitioner that a stated amount of the drug be dispensed for a person who is or will be named in the authorization. SOR/78-154, s

Section I: Table of regulations, statutory instruments (other than regulations) and other documents—June 30 2019

http://canadagazette.gc.ca/rp-pr/p2/2019/2019-06-30-c2/section1-eng.html

Aug 26, 2019 ... Act, 2001 Ancillary Activities (Insurance Companies, Canadian Societies and Insurance Holding Companies) Regulations Insurance Companies Act Anhydrous Ammonia Bulk Storage Regulations (General Order No. O-33) Canada Transportation Act Animals of the Family Bovidae and Their Products Importation Prohibition Regulations Health of Animals Act Annex Code 9075

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