The latest updates to Practical Law’s Life Sciences Global Guide feature contributions from Tilleke & Gibbins attorneys in the firm’s Phnom Penh office, who wrote “Medicinal Product Regulation and Product Liability in Cambodia.”
This overview form Practical Law covers a range of regulatory issues related to the marketing and selling of pharmaceutical products, including the following:
- Regulatory overview, including relevant authorities, scope, definitions, and general procedures for pharmaceuticals, biologicals, and medical devices and health care IT
- Pricing, government funding, and reimbursement: Structure of the Cambodian health care system, price regulation, and reimbursement
- Clinical trials
- Manufacturing and distribution
- Marketing: Authorization for marketing medicinal products, parallel imports and cross-border trade in medicines
- Restrictions on dealings with health care professionals
- Selling restrictions
- Advertising and promotion
- Data privacy
- Packaging, labeling, and tracking
- Product safety, quality, and liability
- Local establishment, representation, and residency requirements
- Reform
The full Medicinal Product Regulation and Product Liability in Cambodia chapter can be accessed on the Practical Law website.
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