TGA Checklists (FOI’d documents) 

Below are the TGA FOI Checklist documents for further Committee review and discussion. Documents were received by CMA on 16 March 2023. NOTE: These links only work for logged-in Regulatory Committee members.The documents are currently in the “as-is” received form, except for the document name where I have added the number of pages and a general description of the contents of the document.Please see my reply below for the delegate’s reasons for Redacted Information (s22 or s47) within the documents.Document 1 AR – 4p Targeted Review Label_ Safety_ Name.PDFDocument 2 AR – 31p V4-0 Apr 2020 LCS Label_ Manufacturing_ Evidence.PDFDocument 3 AR – 30p V4-0 Apr 2020 LCS Label_ Manufacturing_ Evidence.PDFDocument 4 AR – 3p Sponsor Response to Proposal to Cancel.PDFDocument 5 AR – 3p Sponsor Response to Cease and Desist.PDFDocument 6 AR – 31p V4-0 Apr 2020 LCS Label_ Manufacturing_ Evidence.PDFDocument 7 AR – 33p V4-0 Apr 2020 LCS Label_ Manufacturing_ Evidence.PDFDocument 8 AR – 34p Targeted Review of Caffeine.PDFDocument 9 AR – 4p Targeted Review Andrographis.PDFDocument 10 AR – 3p ARTG Scanning.PDFDocument 11 AR – 5p ARTG Scanning – Medicine Name.PDFDocument 12 AR – 8p Targeted Evidence.PDFDocument 13 AR – 4p Label_ Warnings_ Free From.PDFDocument 14 AR – 3p Targeted Review Recall of Fennel products.PDFDocument 15 AR – 2p Assessment of non-compliant goods.PDF
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