의료기기 일괄허가 및 기술문서 심사를 위한 품목별 길라잡이 개발 = Preparation of guidance documents item by item for one-step evaluation and approval for Medical Devices

다국어 초록 (Multilingual Abstract)

Approvals of medical device increase every year as industry of medical device grows. Therefore KFDA keeps trying to improve approval systems. However, the firms of medical device are in trouble due to regulation amendment, a firm of small size, exchange of the person in charge. The staffs of KFDA increase their work load because applicants of approval of medical device aren't used to writing of document. Therefore the firm of medical device in business have a long term.
KFDA develops eight guidance document item by item for one-step evaluation and approval for Medical Devices because applicants of approval of medical device write documents easily. KFDA reviewer can carry on quick reviewing in use of this eight guidances. This guidance are improved on satisfaction of applicants of approval of medical device.

참고문헌 (Reference)

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17 "ASTM F 881-94 Standard Specification for Silicone Elastomer Facial Implants"

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