Medicines Registration is the strictest process in CFDA. BDe consulting has the experienced specialists in order to be successful handle the registration projects in China. The specialists work closely with our clients, coordinating the submission of regulatory documents, answering CFDA follow up questions and providing clinical trail in China.
The scope of project will include:
Determine Drug classification;
Ascertain the best route to CFDA approval in China;
Development of a Product Registration Standard;
Follow up type testing;
Obtain registration certificate.