Sign for Notice Everyday    Sign Up| Sign In| Link| English|

Our Sponsors

    Receive Latest News

    Feedburner
    Share Us


    Regulatory Requirements for Registration of Medical Device Products in China

    View: 144

    Website https://worldcomplianceseminars.com/upcoming_webinar | Want to Edit it Edit Freely

    Category CRO’s • Regulatory Affairs • RA Specialists • Clinical Affairs • Quality Control/Quality Assurance • Compliance • Marketing & Sales • Distributors/Authorized Representatives • Engineering/Technical Services • Consultants • Manufacturing • Auditors

    Deadline: March 17, 2020 | Date: March 17, 2020

    Venue/Country: U.S.A

    Updated: 2020-01-06 15:53:39 (GMT+9)

    Call For Papers - CFP

    Overview:

    Entering the Chinese market offers tremendous opportunity for medical device companies, but it is not without challenges. Although China’s medical regulatory bodies are becoming more harmonized with international standards, the Chinese registration process still poses significant difficulties for Western medical device and pharmaceutical firms.

    In China, it can also become difficult to make a clear distinction between your regulatory strategy and business strategy. Learn how to prepare the necessary documents and register your product with the Chinese regulatory authorities


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.