Made-in-China Strategy
While clinical trial is your only pathway of clinical evaluation, GVMMedicalTM RA team and CRO team will work together to help you to identify the minimum regulatory requirement. Besides preparation the Clinical trial protocols for you, our CRO team is also very experienced to manage your clinical trial process and prepare the clinical trial report.
Order 104 Pathway
You are the king. Let us know your target and your concerns. Talk about your products.
MAH Pathway
China has so many innovative programs. Our US team will collaborate with China team to match your case to the best pathway for you.
You are the king. Let us know your target and your concerns. Talk about your products.
QUESTIONS?
Whether you’re curious about a free talk, or even press, we’re here to answer any questions.
GVM MedTech RA/QA Service
Why Choose US
Good Knowledge
We dedicate to study the regulation update context that we provide you the accurate insight of the regulations.
Bilingual & Cross-Cultural Experts
Our project manager (PM), business development rep (BD), and part of the experts have background working in US and China.
A network of industry experts
The diversity of the medical device industry makes expert networks extremely important
Hard Working
We respect your time and money, our U.S. and Chinese teams worked together to create a 7/24 rhythm. We will try our best to keep your project proceed in a timely manner.