The latest update to Practical Law’s Life Sciences Global Guide includes a new “Life Sciences Regulation in Thailand” chapter by attorneys in Tilleke & Gibbins’ Bangkok office. The chapter covers a range of regulatory issues related to development, manufacturing, and selling of pharmaceutical products and medical devices in Thailand. The chapter provides important information on 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
• Developments, reforms, and 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 Thailand” chapter can be accessed on the Practical Law website.