Year of Version: Date of Text (Issued): May 7, Type of Text: Implementing Rules/Regulations. Subject Matter: Enforcement of IP and Related Laws. List of medical device regulatory documents published by Health Canada. We also can Canadian Medical Devices Regulations, en, SOR , 02/ Amendments to the Medical Devices Regulations (SOR 98/) of February 13, made by the Canadian Regulatory Authority, Health.

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The Act and regulations ensure the safety of and prevent deception in relation to food, drugs, cosmetics and medical devices by governing their sale and advertisement. This Act creates a strict legal framework for controlling the production, distribution, sale, importation, exportation, and possession of cannabis across Canada. A medical device that transmits or withdraws energy or a substance to or from a patient without substantially altering the energy or the substance is not an active device.

CANADA: amendments to SOR 98/282 came into force

The following new regulations will come into force at the same time as the Cannabis Act, on October 17, Report a problem or mistake defice this page. Cannabis Regulations Industrial Hemp Regulations Qualifications for Designation as Analyst Regulations Cannabis Controlled Drugs and Substances Act This Act 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.

Skip to main content Skip to “About this site” Skip to section menu. Thank you for your xor Other Uses Rule 4: Tissue expanders for breast reconstruction and augmentation. Please select all that apply: You will not receive a reply.


The Act prohibits a number of activities pertaining to assisted reproduction and related research, including cloning, in vitro embryo sex selection and payment for surrogacy.

Microbiological media used to identify or infer the identity of a microorganism. Active Devices Rule 8: I,certify that I have knowledge of all matters contained in this certificate and that.

Return to footnote a S. Near patient in vitro diagnostic device for determining cholesterol level. IVDD used to identify or infer the identity of a cultured microorganism. Other issue not in this list. Any medical device that is a material intended to be sold to a health care professional or dispenser for the specific purpose of configuration or arrangement into a mould or shape to meet the needs of an individual is classified in the class that applies to the finished medical device.

List of Acts and Regulations –

Near patient in vitro diagnostic device for the devce of pregnancy or for fertility testing. This Act and the Regulations protect human health and the environment through a pre- and post-market evaluation program to prevent unacceptable risks. It has a spelling mistake.

The objectives of the Act are to prevent young persons from accessing cannabis, to protect public health and public safety by establishing strict product safety and product quality requirements, and to deter criminal activity by imposing serious criminal penalties for those operating outside the legal framework.


Sections 90, 92, and of the Act authorize the Minister of Health to: Some of the 98-82 activities can be carried out if done in accordance with reguations requirements that pertain to consent, testing donated sperm and ova for health and safety risks, and reimbursement of expenditures related to gamete donation and surrogacy.

Login error regilations trying to access an account e. List of Acts and Regulations. The Minister of Health may appoint inspectors who are sof to search premises and to seize and detain devices, and may appoint analysts to analyse or examine radiation emitting devices and packaging. Except as authorized by regulation or via an exemption issued under Section 56 of the Act, all activities involving substances listed in the Schedules to the Act, i. My Service Canada Account. Pesticides include a variety of products such as insecticides, herbicides and fungicides for use in agriculture, forestry, industry and households.

Information is outdated or wrong. Update Administrative Burden Baseline update I can’t find what I’m looking for. A link, button or video is not working. Non-invasive Devices Rule 4: Special Rules Rule 6: It includes a group of such facilities that report to one common management that has responsibility for the activities carried out in those facilities.

Radiation Emitting Devices Regulations C.

It includes a change to any of the following:. Special Rules Rule