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 5692 record(s)

Req # A-2023-0021

Data relating to variations in CIHR’s budget dedicated to graduate student scholarships, for the period of 2007-2008 to 2023-2024.

Organization: Canadian Institutes of Health Research

0 page(s)
April 2024

Nothing to report this month

Organization: Canada Hibernia Holding Corporation

April 2024

Req # A-2023-00004

A digital, machine-readable copy of passenger complaints at YUL (Montreal airport) from Jan. 1, 2020 to June 12, 2023

Organization: Canadian Air Transport Security Authority

381 page(s)
March 2024

Req # A-2019-0013

All data and emails received and/or prepared from March 1, 2019 until December 2, 2019 regarding vaping related illnesses.

Organization: Canadian Institutes of Health Research

431 page(s)
March 2024

Req # A-2021-0021

All reports, briefing notes, budgets, and emails/correspondence pertaining to the New Brunswick Cluster of Neurological Syndrome of Unknown Cause, produced between January 1, 2020, and Nov 18, 2021.

Organization: Canadian Institutes of Health Research

1099 page(s)
March 2024

Req # A-2022-0008

All records about how CIHR has responded to reports that the Canadian Common CV (Curriculum Vitae) has obstacles that impede disabled individuals from equal participation, from January 1, 2018 to May 14, 2022.

Organization: Canadian Institutes of Health Research

298 page(s)
March 2024

Req # A-2016-000420

Documents relating to Health Canada’s approval of INFLECTRA (Drug Identification Number (DIN) # 02419475): All Health Canada reviewers reports and reviewer comments; and all minutes from any pre-Supplement to a New Drug Submission (SNDS) meetings between Celltrion (health care company) and Health Canada between September 1, 2014 and June 30, 2015.

Organization: Health Canada

299 page(s)
March 2024

Req # A-2019-001464

All domestic Adverse Drug Reaction (ADR) reports for Tetanus, Diphtheria and Pertussis (Tdap) Hepatitis B, Measles, Mumps and Rubella (MMR), Varicelli, Inactivated Polio Vaccine (IPV), Diphtheria, Tetanus and Pertussis (DTaP), Flu for the period of October 1, 2018 - end of March 2019.

Organization: Health Canada

3917 page(s)
March 2024

Req # A-2019-001525

The Clinical Overview, Clinical Summary of Efficacy and Clinical Summary of Safety submitted to Health Canada as part of the Supplemental New Drug Submission (SNDS) (control number: 204690; decision date: 2018-03-29) in respect of TALTZ.

Organization: Health Canada

898 page(s)
March 2024

Req # A-2020-001374

For the period 2015 to April 19, 2021, and in relation to natural health product brand names containing the phrase “glucosamine sulfate” or “glucosamine sulphate”, with license holders named WN Pharmaceuticals Ltd, Natural Factors Nutritional Products Limited, or Jamieson Laboratories Inc., the following documents. All product licences, and the specifications to which the natural health product will comply. All applications for a product licence, correspondences with respect to those applications, and the attestations by the applicants that the product will be manufactured and distributed in accordance with good manufacturing practices. All testing done of the product, and correspondences made in relation to the testing of the product. All correspondences between the Minister and a licensee, manufacturer, importer or distributer to stop their sale of the product. All correspondences in relation to labelling and packaging of the product; and all complaints of non-compliance in respect of the product. For the period May 6, 2004 to April 19, 2021, all monographs of “glucosamine sulfate” and “glucosamine hydrochloride”

Organization: Health Canada

1565 page(s)
March 2024
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