Consulting
Description
Your organization wants to show responsibility by making sure that its facilities, equipment, products and services comply with quality, health & safety, whether they are based on sector applicable codes or regulations or specific requirements or recognized international standards, such as China Medical Device GMP, ISO 13485:2003, MDD 93/42/EEC, CMDCAS, 21 CFR 820 , Etc.
Quality and safety are keys for your products. So it is of vital importance to check through inspection in factory the quality of every single item, no matter how small. These items range from raw material to finished products. Any purchase carries embedded risk. If a part is faulty, but the fault is not detected, the risk of something going wrong becomes embedded within the new asset.
Osmunda has rich factory inspection experience and could provide you with the best comprehensive services. We are able to carry out inspections of your facilities, equipment and products, and audits of your systems and processes against practically any referential.
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Osmunda Medical Device Consulting CO.LTD
medical device registration co
Address: 7th Floor,JinGui business center,CongYun road No.982,Baiyun,
Guangzhou, Guangdong
China,
Tel: 0086-020-62321333
Fax: