Open Government Portal

Found 10 records similar to HPFB - Summary Reports (SBD/RDS/SSR) API Database

Federal

Understand the decisions to approve or not approve the sale of drugs and medical devices in Canada.

Last Updated: Sep. 17, 2020
Date Published: Oct. 23, 2016
Organization: Health Canada
Formats: HTML
Keywords:  Regulatory decision, drug and health product review and approval, sale of drugs and medical devices.
Federal

MDALL contains product-specific information on all medical devices that are currently licensed for sale in Canada, or have been licensed in the past.

Last Updated: May 15, 2020
Date Published: Feb. 28, 2018
Organization: Health Canada
Formats: XML JSON HTML
Keywords:  MDALL, therapeutic products, medical devices, active, inactive, licences, company, device, device identifier
Federal

Medical devices imported into Canada for sale, with or without a monetary contribution, must meet Health Canada requirements for commercial importation, as outlined in the Food and Drugs Act (FDA) and the Medical Devices Regulations (MDR).

Last Updated: Apr. 26, 2021
Date Published: Mar. 19, 2021
Organization: Health Canada
Formats: HTML
Keywords:  Guide, regulatory requirements, importing medical devices, commercial importation
Federal

Summary of the results associated with the data collected on student tobacco, alcohol, and drug use for 2018-19.

Last Updated: Mar. 25, 2021
Date Published: Dec. 31, 2019
Organization: Health Canada
Formats: HTML
Keywords:  summary, results, Canadian, students, tobacco, alcohol, drugs, cigarette, cannabis
Federal

Drug and medical device manufacturers submit clinical information to Health Canada for the approval of new products. Health Canada assesses this clinical information to reach a decision on whether or not to approve a drug or medical device.

Last Updated: Sep. 17, 2020
Date Published: Feb. 28, 2019
Organization: Health Canada
Formats: HTML
Keywords:  Clinical information, approval of new drug and health products.
Federal

This notice explains under which circumstances non-medical masks or face coverings would be subject to the regulatory framework for medical devices during the COVID-19 pandemic.

Last Updated: Aug. 28, 2020
Date Published: Jul. 24, 2020
Organization: Health Canada
Formats: HTML
Keywords:  COVID-19 pandemic, Notice to industry, regulatory framework for medical devices, non-medical masks, face coverings.
Federal

Summary of Charges Disposed of at Summary Trial

Last Updated: Mar. 31, 2021
Date Published: Mar. 30, 2021
Organization: National Defence
Formats: CSV
Keywords:  law, statistics, reports
Federal

The updated regulations will help drug makers understand what information should be included in their drug submissions. This will help with product approval and availability.

Last Updated: Sep. 17, 2020
Date Published: Feb. 16, 2018
Organization: Health Canada
Formats: HTML
Keywords:  Improving access to generic drugs, regulatory review of drugs and devices.
Federal

The number and percentage of adjudication decisions and recommendations that are made within legislated time limits and service standards.

Last Updated: Nov. 23, 2020
Date Published: Nov. 23, 2020
Organization: Canada Energy Regulator
Formats: CSV
Keywords:  adjudication, decision, decisions, percentage, process, recommendation, recommendations, legislated time limits, legislated
Federal

This project will build new review pathways for those drugs shown to meet health care system needs. The outcome for the people of Canada will be faster access to drugs, including drugs for rare diseases.

Last Updated: Sep. 17, 2020
Date Published: Feb. 16, 2018
Organization: Health Canada
Formats: HTML
Keywords:  Priority review, faster access to drugs, health care system needs.
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