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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