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 369 record(s)

Req # A-2021-000561

Adverse Reaction Reports (AERs) for CABAZITAXEL. Report numbers: E2B_03413381, E2B_03413387, 000926786.

Organization: Health Canada

25 page(s)
September 2021

Req # A-2021-000563

Adverse Reaction Reports (AERs) for ALEMTUZUMAB. Report numbers: E2B_03394016, E2B_03393987, E2B_03387869, E2B_03391239, E2B_03454376, E2B_03387914, E2B_03391267, E2B_03396602, E2B_03387903, E2B_03391347, E2B_03391236, E2B_03393768, E2B_03392200, E2B_03393774, E2B_03391849, E2B_03391274, E2B_03463382, E2B_03468912, E2B_03387890.

Organization: Health Canada

463 page(s)
September 2021

Req # A-2021-000589

Adverse Reaction Reports (AERs). Report numbers: E2B_03442035, E2B_03625223, 000934948, 000940688, E2B_03037711, E2B_03787485, E2B_03823366.

Organization: Health Canada

108 page(s)
September 2021

Req # A-2021-000602

The Class II Medical Device known as MEDLY. This product was apparently issued Medical Device Licence No.: 104447 on 2020-03-13. The quality management system (QMS) certificate submitted with the licence application in fulfillment of section 32(2)(f) of the Medical Devices Regulations. Information Requested: copy of the certificate described above.

Organization: Health Canada

2 page(s)
September 2021

Req # A-2021-000604

Briefing note in the Ministerial Executive Correspondence System (MECS) for the following file: 19-075631-61.

Organization: Health Canada

27 page(s)
September 2021

Req # A-2021-000622

Briefing note in the Ministerial Executive Correspondence System (MECS) for the following file: 21-075079-338.

Organization: Health Canada

25 page(s)
September 2021

Req # A-2021-000634

Adverse Drug Reaction (ADR) for METFORMIN HYDROCHLORIDE. Report number: E2B_03420918.

Organization: Health Canada

29 page(s)
September 2021

Req # A-2021-000648

Adverse Drug Reaction (ADR) for CANDESARTAN. Report number: E2B_03406743.

Organization: Health Canada

11 page(s)
September 2021

Req # A-2021-000649

Adverse Drug Reaction (ADR) for CLONAZEPAM. Report number: E2B_03468382.

Organization: Health Canada

22 page(s)
September 2021

Req # A-2021-000650

Adverse Reaction Reports (AERs) for CYCLOPHOSPHAMIDE. Report numbers: 918864, 918869, 918929.

Organization: Health Canada

6 page(s)
September 2021
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