제품
?ㅻ━肄섎갭由??ㅽ??쇱쓽 QMS, ?섏?留?FDA 洹쒖젙 以€?? (Silicon Valley UX. FDA Compliance.)
?먮━怨?臾닿굅???덇굅??Legacy) QMS???딆쑝?몄슂. **Harmonizer**???ㅽ??몄뾽??利됱떆 ?꾩엯?????덈뒗 媛€??媛€蹂띻퀬 媛뺣젰??FDA QMSR 諛?ISO 13485 ?몄쬆 ?꾩옄 ?덉쭏 ?쒖뒪?쒖엯?덈떎.
Pre-Validated
FDA Part 11(?꾩옄 ?쒕챸) ?붽뎄?ы빆???€???대? 寃€利?Validation)???꾨즺?섏뼱 ?덉뼱, ?ㅼ튂 利됱떆 媛먯궗(Audit) 以€鍮꾧? ?앸궔?덈떎.
Smart Interactions
遺덈쭔(Complaint)???묒닔?섎㈃ ?먮룞?쇰줈 ?꾪뿕 愿€由?Risk) ??ぉ???낅뜲?댄듃?섍퀬, CAPA ?꾨줈?몄뒪瑜??몃━嫄고빀?덈떎.
DocuSign Integration
蹂꾨룄???꾩옄 ?쒕챸 ???놁씠, ?듭닕??DocuSign 寃쏀뿕 洹몃?濡??뱀씤 ?꾨줈?몄뒪瑜?吏꾪뻾?????덉뒿?덈떎.
자주 묻는 질문
Q. ?꾩엯?섎뒗 ???쇰쭏??嫄몃━?섏슂?
A. ?ъ쟾 援ъ텞??Pre-configured) ?쒗뵆由우쓣 ?ъ슜?섎㈃ 2二??덉뿉 ?꾩엯 媛€?ν빀?덈떎.
Q. 湲곗〈 醫낆씠 臾몄꽌???대뼸寃??섎굹??
A. ?ㅼ틪?섏뿬 'Legacy Records'濡??쇨큵 ?낅줈?쒗븯怨??몃뜳?깊빐 ?쒕┰?덈떎.
Q. 諛몃━?곗씠??蹂닿퀬?쒕? 二쇰굹??
A. ?? FDA ?쒖텧???뚰봽?몄썾??寃€利?蹂닿퀬??Validation Report) ?⑦궎吏€瑜?臾대즺濡??쒓났?⑸땲??