Top Industry News
- FDA Advances New Guidelines for Analysis of Clinical Trials Evaluating Safety of Drug and Biologic Products
- EMA Revises Guidance on Publication of Clinical Trials Policy
- Medsafe (New Zealand)- Clinical Trial Regulatory Approval and Good Clinical Practice Requirements (Updated Guidelines)
- FDA Finalizes Guidance on Mandatory Recall Authority
- Health Canada Drafts Policies on 3D-Printed Implantable Devices
- Anvisa- Guide guides on Food Shelf Life, which is Mandatory in the Labeling of Packaged Products
- EMA- Guideline on Quality Aspects Included in the Product Information for Vaccines for Human use
- Swissmedic - Current status for Approvals of Homeopathic and Anthroposophic Medicines without Indication
- EMA- Guideline on Good Pharmacovigilance Practices (GVP)
- EMA- Guideline on the Requirements for Quality Documentation Concerning Biological Investigational Medicinal Products in Clinical Trials