Update a Guidance document form
Please complete this form to inform us of any GHTF or IMDRF guidance documents you believe need updating. All fields are compulsory.
Member websites
- Australia - Therapeutic Goods Administration
- Brazil - National Health Surveillance Agency (ANVISA)
- Canada - Health Canada
- European Union - European Commission Directorate General Health and Consumers
- Japan - Pharmaceuticals and Medical Devices Agency
- Japan - Ministry of Health, Labour and Welfare
- USA - US Food and Drug Administration