China Life Sciences Lawyer — Pharmaceutical & Medical Device Regulation
Director Li Maoshu | Life Sciences, Healthcare & Pharmaceutical Regulatory Compliance
17I Shangbu Building, Futian, Shenzhen | Guangdong Faniu Law Firm
Life Sciences Legal Services in China
China's life sciences sector is undergoing rapid transformation. With regulatory reforms accelerating drug approvals and medical device registrations, companies need experienced legal counsel to navigate this complex landscape.
Guangdong Faniu Law Firm provides specialized legal services for life sciences companies:
- Drug and medical device registration and market access
- Clinical trial agreements and regulatory compliance
- Intellectual property protection for pharmaceuticals
- Technology licensing and technology transfer agreements
- Manufacturing and distribution agreements
- Regulatory investigations and enforcement defense
Director Li Maoshu understands the unique challenges life sciences companies face in China. From innovative startups to multinational pharmaceutical corporations, we provide practical, risk-based legal advice.
Call 18664921865 for a free initial consultation on your life sciences legal needs.
Frequently Asked Questions
How long does drug registration take in China?
NMPA drug registration typically takes 12-36 months. Priority review pathways exist for innovative drugs and drugs addressing unmet medical needs.
Can foreign clinical trial data be used for China registration?
Yes, NMPA accepts foreign clinical trial data under certain conditions. A bridging study in Chinese patients may still be required depending on the product.
What are the IP protection options for pharmaceuticals?
Patent protection (20 years), data exclusivity (6 years for innovative drugs), and trademark protection are available. Patent linkage and patent term extension systems are being implemented.
More questions? Call 18664921865 Director Li Maoshu for free answers