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.
For further information, please contact:
Hien Thi Thu Vu, Tilleke & Gibbins
thuhien.v@tilleke.com
