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Results for: "Medical" and "device" and "SFDA" and "Registration" and "China"
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| 0 | Sell | Condition for Design of Clinical Trial Plans
Osmunda Medical Device Consulting Organization, the largest and most professional consulti... Osmunda Medical Device Consulting Organization, the largest and most professional consulting comp... ...ical device quality system certification and product registration, such as SFDA registration, QSR 820 system, FDA registration, ISO 13485 system, CE certi... ...des global various medical device quality system certification and product registration, such as SFDA registration, QSR 820 system, FDA registration, ISO 13485 sy... ...and most professional consulting company in the field of medical device in China, provides global various medical device quality system certification and p...
Posted on: 2012-12-07 from China - Guangdong
|  | | 0 | Sell | Medical device registration consulting
Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (Sta... Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (State Food... ...ended use, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di... ...e, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be regis...
Posted on: 2012-08-13 from China - Guangdong
| | | 0 | Sell | SFDA Registration Consulting
Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (Sta... Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (State Food... ...ended use, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di... ...e, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be regis...
Posted on: 2012-08-13 from China - Guangdong
| | | 0 | Sell | SFDA IVDD Registration in China
...ening and adopting radioisotope labeling, other IVDD need to be managed as medical device (MD). IVDD is divided into three management categories according to... ...d adopting radioisotope labeling, other IVDD need to be managed as medical device (MD). IVDD is divided into three management categories according to its ri... ... in addition to the general regulations of medical device. During the SFDA registration, the class 2 and class 3 of IVDD are required to conduct clin... ...ing to its risk level. There are some special requirements during the IVDD registration in addition to the general regulations of medical device. During the ... Currently in China, except the in vitro diagnostic reagents (IVDD) which used for blood scree...
Posted on: 2012-08-13 from China - Guangdong
| | | 0 | Sell | Medical device SFDA Registration in China
Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (Sta... Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (State Food... ...ended use, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di... ...e, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be regis...
Posted on: 2012-08-13 from China - Guangdong
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| | 0 | Sell | Medical device SFDA Registration in China
Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (Sta... Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (State Food... ...ended use, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di... ...e, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be regis...
Posted on: 2012-06-28 from China - Guangdong
| | | 0 | Sell | SFDA Registration
Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (Sta... Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (State Food... ...ended use, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to... ...on). All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China. Di... ...e, medical devices are divided into three management categories by SFDA of China (State Food and Drug Administration). All medical devices need to be regis...
Posted on: 2012-06-08 from China - Guangdong
| | | 0 | Sell | SFDA Registration services
Services we provide: medical device registration consulting, ISO13485certification consulting, medical ... Services we provide: medical device registration consulting, ISO13485certification consulting, medical equipme... ...tralian TGA registered consulting, Japan JPAL registered consulting, China SFDA registration, medical equipment GMP certification ， the second part... Services we provide: medical device registration consulting, ISO13485certification consulting, medical equipment certificat... ...g, Australian TGA registered consulting, Japan JPAL registered consulting, China SFDA registration, medical equipment GMP certification ， the second...
Posted on: 2012-06-07 from China - Guangdong
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