Registration for MD and IVD reagents in CFDA includes registration test, clinical trial and products registration. Registration test is the first step.
More than 10 years’ experience with registration testing in Beijing,Tianjin,Hangzhou,Shanghai and other testing institute designated by CFDA, Haimiao provide services as followed:
1. Draft product standards/technical requirements.
2. According to product characteristics and test requirements, guide customers to provide the corresponding file, instrument, reagents and various components.
3. Communicate with testing engineer and track products’ test in relative testing institute.
4. Get test report.
Test period:45-60 working days
