REGULATORY AFFAIRS
Your regulatory partner that guides you through your product’s registration journey, helping to accelerate market entry for faster patient access
With local regulatory affairs teams in 13 territories across Asia, Zuellig Pharma offers regulatory services that are up to date with the ever-changing local regulations, making the products available for patients in need and ensuring regulatory compliance for a smooth product commercialisation.
Throughout our years of experience with more than 3,000 product registrations and marketing authorisation transfer approvals across the region, we have established best practices to identify regulatory pitfalls and increase projection accuracy for the successful commercialisation of new products.
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Thank you for your interest in our services. Please email us at ZPRegionalRegulatory@zuelligpharma.com with the following information:
- Company Name
- Company Overview
- Category of Product
- Service of Interest
- Country of Interest
