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 7280 record(s)

Req # A-2023-001527

As of December 15, 2023, there are now two liraglutide submissions which appear on the Generic Submissions Under Review (GSUR) List. Provide the name of the company who submitted the Abbreviated New Drug Submission (ANDS); and the year and month in which the ANDS was accepted for review.

Organization: Health Canada

1 page(s)
May 2024

Req # A-2023-001536

As part of its application to Health Canada for authorization to sell the COVID-19 lateral flow device with the Interim Order (IO) authorization Identification 327866, the manufacturer sent the federal government about 200 sample tests. Provide the report that the Health Canada team led by the Director General received from the National Microbiology Laboratory on the test's accuracy and considered as they evaluated the application, approving it on October 20, 2021.

Organization: Health Canada

8 page(s)
May 2024

Req # A-2023-001537

As part of its application to Health Canada for authorization to sell the three COVID-19 lateral flow devices with the Interim Order (IO) authorization Identifications 313054, 328889, and 333956, the manufacturer sent the federal government about 200 sample tests for each one. Provide the reports that the Health Canada team led by the Director General received from the National Microbiology Laboratory on the tests' accuracy andconsidered as they evaluated the applications, approving the three devices respectively in February, June and December 2021.

Organization: Health Canada

8 page(s)
May 2024

Req # A-2023-001572

Any security related training completed by Nadine Huggins, the Senior Assistant Deputy Minister (ADM) and Chief Security officer at Health Canada.

Organization: Health Canada

90 page(s)
May 2024

Req # A-2024-000099

The Public Health Agency of Canada’s (PHAC) submission or related communications that were provided to the Patented Medicine Prices Review Board (PMPRB) in response to its November 2022 Consultation on the Board’s Guidelines.

Organization: Health Canada

17 page(s)
May 2024

Req # A-2020-001326

Briefing note in the Ministerial Executive Correspondence System (MECS) for the following file: 20-112741-953.

Organization: Health Canada

14 page(s)
May 2024

Req # A-2020-001891

Adverse Drug Reactions (ADRs) for Pantoprazole sodium. Report numbers: E2B_03353411, E2B_03373956. ADRs for Tecta. Report numbers: E2B_03380105, E2B_03402109. ADRs for Pantoprazole magnesium. Report numbers: 921752, E2B_03380218. ADRs for Amphetamine aspartate monohydrate/ amphetamine sulfate/ dextroamphetamine saccharate/ dextroamphetamine sulfate. Report numbers: E2B_03355369, 921791, E2B_03385512.

Organization: Health Canada

276 page(s)
May 2024

Req # A-2021-001088

Briefing note in the Ministerial Executive Correspondence System (MECS) for the following file: 21-106818-522.

Organization: Health Canada

73 page(s)
May 2024

Req # A-2021-001202

Adverse Drug Reactions (ADRs). Report numbers: E2B_03487061, E2B_03487072, E2B_03487074, E2B_03487077, E2B_03490042, E2B_03490043, E2B_03490045, E2B_03490049, E2B_03490050, E2B_03491975, E2B_03492634, E2B_03492652, E2B_03495037, E2B_03524901, E2B_03542686, E2B_03606495, E2B_03614104, E2B_03622423, E2B_03638865, E2B_03867292.

Organization: Health Canada

330 page(s)
May 2024

Req # A-2021-001291

Adverse Drug Reactions (ADRs). Report numbers: 000923457, E2B_03206897, 000938466, 000949183, 000956295, E2B_03838745, E2B_03998278, E2B_03081668, E2B_03840368, E2B_03940910, E2B_02771636, E2B_02836652, E2B_02836886, E2B_03503549, E2B_02758454, E2B_03320166, 000927161, 000721376, E2B_01656713, E2B_02461795.

Organization: Health Canada

384 page(s)
May 2024
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