Completed Access to Information Requests

About this information

Search the summaries of completed Access to Information (ATI) requests to find information about ATI requests made to the Government of Canada after January 2020. If you find a summary of interest, you can request a copy of the records at no cost using the form below each summary. Requests made through this form are considered informal requests and are not subject to the same requirements as requests under the Access to Information Act (ATIA).

If you don’t find what you are looking for you can request additional government records under an institution’s control by contacting the institution’s Access to Information and Privacy Coordinator or by submitting a formal access to information request.

*All information provided will incorporate the necessary exemptions and exclusions as per the Access to Information Act and the Privacy Act.

Download datasets of the summaries of completed access to information requests.

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Found 5820 record(s)

Req # A-2021-000819

The Signal Assessment: Typical (conventional) antipsychotics and All-cause Mortality (2009).

Organization: Health Canada

73 page(s)
September 2022

Req # A-2021-000937

Information on a product presently considered for access by Health Canada's Special Access Program (SAP). All products containing PSMA-11. Both 68Ga-labelled and 18F-labelled. The following information from requests made for the period…

Organization: Health Canada

19 page(s)
September 2022

Req # A-2021-001240

According to the Health Canada Generic Submissions Under Review List, an Abbreviated New Drug Submission (ANDS) for degarelix acetate was submitted on or after October 1, 2018. Documents containing information regarding the mock-ups of every label…

Organization: Health Canada

475 page(s)
September 2022

Req # A-2021-001288

Disclosable Good Manufacturing Practices (GMP) inspection document(s) listing the Inspector’s detailed observations, conditions found, and any follow-up expected by Health Canada for the drug establishment licence GMP foreign evidence inspection of…

Organization: Health Canada

14 page(s)
September 2022

Req # A-2021-001768

The source data used in making policies related to mandatory vaccination against COVID-19 travel restrictions, namely in regard to the requirement for vaccination in order to travel within and out of Canada. All the data that the government relies…

Organization: Health Canada

0 page(s)
September 2022

Req # A-2021-001959

Respecting ATIA requests A-2021-000734, A-2021-001017, and A-2021-001140, please provide the following records: Health Product and Food Branch (HPFB) recommendations, and summary documents thereof, completed Extension Justification Form(s), records…

Organization: Health Canada

71 page(s)
September 2022

Req # A-2022-000243

Health Canada issued a public advisory (Identification #RA-64122) on April 28, 2022 advising that Apotex Inc. is recalling five lots of Apo-Acyclovir tablets, in 200 mg and 800 mg strengths, due to the presence of N-nitrosodimethylamine (NDMA) above…

Organization: Health Canada

10 page(s)
September 2022

Req # A-2022-000257

The number of rapid tests distributed to government employees by department for each month and for each product type since September 2020. The number of rapid tests distributed to the private sector by organization during the same timeframe.

Organization: Health Canada

45 page(s)
September 2022

Req # A-2022-000371

The Health Canada approval letter for Vertex Pharmaceutical's trial to be carried out in Canada: A Safety, Tolerability, and Efficacy Study of VX-880 in Participants With Type 1 Diabetes (ClinicalTrials.gov Identifier: NCT04786262).

Organization: Health Canada

4 page(s)
September 2022

Req # A-2022-000391

Cover letter indicating the brand name of the reference drug product and the dosage form of the generic drug in Health Canada’s list of “Generic Drug Submissions Under Review” dated 2022-06-22 for the medicinal ingredient buprenorphine. Screening…

Organization: Health Canada

4 page(s)
September 2022
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