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Arazy Group is a medical device consultant based in Vancouver region of British Columbia and help medical equipment manufacturers in promoting their products in an international market. We provide registration of medical device in more than 53 countries and some of the important regulatory services offered by us are South Korea KFDA registration, China SFDA approval, Canada CMDCAS compliance, Russia Gost-R, Brazil – ANIVSA clearance, US FDA clearance, EU CE Mark, ANIMAT approval.
If you are looking to market your medical equipments in China then you have to apply for State Food and Drug Administration (SFDA).
SFDA is a medical devices registration certificate that is must for marketing your medical device in China.
We are working in this field for the last 15 years and our clinical and medical research involve clinical literature review, clinical development planning and trial design, clinical study material, clinical research administration and usability studies, and vigilance report.
For any query or more information about medical device registration China, browse the website.
Arazy Group
350 | 1333 Johnston Street | Pier 32 | Granville Island | Vancouver BC | Canada V6H 3R9
Phone: +1 604.681.6888 PST - Vancouver, Canada
E-Mail us: info@arazygroup.com
Website: http://arazygroup.com/medical_device_registration_in_china_
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