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 624 record(s)

Req # A-2023-000167

COVID-19 impact reports of GEN-Clozapine. All marketed strengths of GEN-Clozapine (Drug Identificatoin Number (DIN) #s, 02247243, 02247244, 02305003 and 02305011).

Organization: Health Canada

197 page(s)
October 2023

Req # A-2023-000301

The disclosable inspection document(s) listing the Inspector’s detailed observations, conditions found, and any follow-up expected by Health Canada for the human drugs drug establishment licence Good Clinical Practice (GCP) inspection of the Merck Canada facility in Kirkland, Quebec, for the Region of Alberta starting around 25 May 2021. Reference Number 182348.

Organization: Health Canada

10 page(s)
October 2023

Req # A-2023-000302

The disclosable inspection document(s) listing the Inspector’s detailed observations, conditions found, and any follow-up expected by Health Canada for the human drugs drug establishment licence Good Pharmacovigilance Practices (GVP) inspection of the Bausch & Lomb facility in Rochester, New York, United States of America starting around 6 December 2022. Reference Number 502442.

Organization: Health Canada

39 page(s)
October 2023

Req # A-2023-000303

Provide the disclosable inspection document(s) listing the Inspector’s detailed observations, conditions found, and any follow-up expected by Health Canada for the human drugs drug establishment licence Good Pharmacovigilance Practices (GVP) inspection of the Merck Canada facility in Kirkland, Quebec, starting around 7 November 2022. Reference Number 502785.

Organization: Health Canada

21 page(s)
October 2023

Req # A-2023-000383

All emails between members of the Scientific Advisory Committee on Health Products for Women and/or between members of the Scientific Advisory Committee on Health Products for Women and the committee’s secretariat on the topic of breast implants.

Organization: Health Canada

173 page(s)
October 2023

Req # A-2023-000455

Every final Harassment and Violence investigation report completed during the period of April 1, 2021 to March 31, 2023.

Organization: Health Canada

112 page(s)
October 2023

Req # A-2023-000458

The disclosable inspection document(s) listing the Inspector’s detailed observations, conditions found, and any follow-up expected by Health Canada for the human drugs drug establishment licence Good Manufacturing Practices (GMP) inspection of the Apotex facility on Signet Drive, Toronto, Ontario starting around 5 June 2017. Reference Number 501259.

Organization: Health Canada

9 page(s)
October 2023

Req # A-2023-000473

All relevant documents from the following workstreams: Workstream D: Pollinator protection and neonicotinoid pesticides; Workstream E: Pest control emerging technologies related to the Canada-United States Regulatory Cooperation Council (RCC) for pesticides 2019–2020.

Organization: Health Canada

37 page(s)
October 2023

Req # A-2023-000493

All correspondence between Health Canada and Dr. Robert Casper and/or Toronto Centre for Advance Reproductive Technology (TCART) related to the Ovu Science company and/or AUGMENT intervention or study.

Organization: Health Canada

26 page(s)
October 2023

Req # A-2023-000737

All documents submitted in the medical device license application, resulting in Acro Biotech's Medical Device Licence (MDL)#108387, be provided.

Organization: Health Canada

35 page(s)
October 2023
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