Completed Access to Information Requests

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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). For additional information, please see the “About Access to Information Requests” webpage.

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.

Found 6 record(s)

Req # A-2021-001600

For the Abbreviated New Drug Submission underlying the generic submission under review containing the medicinal ingredient “trabectedin”, provide the proposed Certified Product Information Document.

Organization: Health Canada

0 page(s)
February 2022

Req # A-2021-001601

For the Abbreviated New Drug Submission underlying the generic submission under review containing the medicinal ingredient “trabectedin”, provide the “Batch Formula” (3.2.P.3.2).

Organization: Health Canada

0 page(s)
February 2022

Req # A-2021-001602

For the Abbreviated New Drug Submission underlying the generic submission under review containing the medicinal ingredient “trabectedin”, provide the “Description of Manufacturing Process and Process Controls” (3.2.P.3.3).

Organization: Health Canada

0 page(s)
February 2022

Req # A-2021-001605

For the Abbreviated New Drug Submission underlying the generic submission under review containing the medicinal ingredient “trabectedin”, provide the proposed Product Monograph.

Organization: Health Canada

0 page(s)
February 2022

Req # A-2019-000740

All documents submitted by Sandoz Canada Inc. in Electronic Common Technical Document (eCTD) Module 1.6.1 (Comparative Bioavailability Information) of any Abbreviated New Drug Submissions made by Sandoz Canada Inc. for its GLATOPA product (glatiramer acetate).

Organization: Health Canada

0 page(s)
February 2020

Req # A-2019-001413

All records, from 2015 to November 19, 2019, sent by Imperial Tobacco Canada Limited to Health Canada under the Tobacco Reporting Regulations.

Organization: Health Canada

0 page(s)
February 2020
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