Practitioners from Tilleke & Gibbins’ Vietnam offices contributed content for the latest edition of the Practical Law Life Sciences Global Guide. The guide provides a comparative overview, in Q&A format, of laws and regulations on pharmaceuticals, medical devices, and other life sciences products in dozens of jurisdictions around the world.
The Life Sciences Global Guide is divided into two sections: Commercialization (see more details here) and Regulation, which covers the following topics:
- Pharmaceuticals: Laws and regulatory authorities
- Clinical trials: Legal, regulatory, and procedural requirements
- Manufacturing and distribution
- Marketing: Authorization for marketing medicinal products, monitoring compliance and penalties, pharmacovigilance and other commitments, foreign marketing authorizations
- Data privacy
- Packaging, labeling, and tracking
- Biological medicines
- Medical devices: Legislation and regulatory authorities, definition and classification
- Healthcare IT
- Combination products and borderlines
- Natural health products
- Recent developments and reform proposals
Practical Law, produced by Thomson Reuters, is the world’s leading legal know-how resource for business lawyers, publishing a huge range of guides covering hundreds of jurisdictions and practice areas.
The full “Life Sciences Regulation in Vietnam” section can be found on the Practical Law website.
