With its registered company in China, BaiPharm can be your trusted local authorized agent and provide support throughout the entire lifecycle of your drug product. From product development to its commercialization, we can ensure compliance with China local regulations and provide feasible regulatory guidance. Please contact us for more information on the following services:
Local agent for DMF filing
Local agent for clinical approval application
Local agent for drug registration
Regulatory communication with local authorities
Local agent for applications of product & manufacture process change
Compilation, editing and submission of annual reports
Report adverse reactions to authorities
Local agent for overseas MAH
Why Choose BaiPharm
Our experts have achieved a thorough understanding of pharmaceutical regulations and extensive experience to provide solutions across all critical stages in the drug life cycle. We’re committed to providing clients with professional and customizable pharmaceutical regulatory compliance services, including market access consultation and registration of prescription drugs, OTCs, APIs, excipients and packaging materials. Our constant driver is to ensure high-level professional and efficient solutions for pharmaceutical enterprises across the globe.
