EN These include FDA 21 CFR Part 11, for digital records submitted electronically for regulated FDA filings, and Unique Device Identifier (UDI) requirements for device labels and packages
Tarjamahake "fda" menyang Wong korea
Nuduhake 15 saka 15 terjemahan saka ukara "fda" saka Basa inggris menyang Wong korea
Terjemahan Basa inggris menyang Wong korea saka fda
Basa inggris
Wong korea
KO 여기에는 FDA 규제 기록을 위해 전자 방식으로 제출되는 디지털 기록 및 장치 라벨 및 포장에 대한 고유 장치 식별자(UDI)에 대한 FDA 21 CFR 파트 11이 포함됩니다
Transliterasi yeogieneun FDA gyuje gilog-eul wihae jeonja bangsig-eulo jechuldoeneun dijiteol gilog mich jangchi label mich pojang-e daehan goyu jangchi sigbyeolja(UDI)e daehan FDA 21 CFR pateu 11i pohamdoebnida
EN These include FDA 21 CFR Part 11, for digital records submitted electronically for regulated FDA filings, and Unique Device Identifier (UDI) requirements for device labels and packages
KO 여기에는 FDA 규제 기록을 위해 전자 방식으로 제출되는 디지털 기록 및 장치 라벨 및 포장에 대한 고유 장치 식별자(UDI)에 대한 FDA 21 CFR 파트 11이 포함됩니다
Transliterasi yeogieneun FDA gyuje gilog-eul wihae jeonja bangsig-eulo jechuldoeneun dijiteol gilog mich jangchi label mich pojang-e daehan goyu jangchi sigbyeolja(UDI)e daehan FDA 21 CFR pateu 11i pohamdoebnida
EN TIBCO provides extensive support for enterprise governance in industries like finance, healthcare, insurance, manufacturing, and pharma, including ISO 9001, FDA 21 CFR Part 11 and GxP, GDPR, and CCPC.
KO ISO 9001, FDA 21 CFR Part 11 및 GxP, GDPR 및 CCPC를 포함한 금융, 의료, 보험, 제조 및 제약 등의 산업에서 엔터프라이즈 거버넌스를 광범위하게 지원합니다.
Transliterasi ISO 9001, FDA 21 CFR Part 11 mich GxP, GDPR mich CCPCleul pohamhan geum-yung, uilyo, boheom, jejo mich jeyag deung-ui san-eob-eseo enteopeulaijeu geobeoneonseuleul gwangbeom-wihage jiwonhabnida.
| Basa inggris | Wong korea |
|---|---|
| iso | iso |
| gdpr | gdpr |
EN Pfizer’s COVID-19 vaccine is authorized by the FDA for kids aged 12 and up. It was found to be safe and effective in protecting children as young as 12 in clinical trials.
KO Pfizer의 COVID-19 백신은 12세 이상 아동을 대상으로 FDA의 승인을 받았습니다. 임상 시험을 통해 12세 이상의 어린이를 안전하고 효과적으로 보호한다는 것이 확인되었습니다.
Transliterasi Pfizerui COVID-19 baegsin-eun 12se isang adong-eul daesang-eulo FDAui seung-in-eul bad-assseubnida. imsang siheom-eul tonghae 12se isang-ui eolin-ileul anjeonhago hyogwajeog-eulo bohohandaneun geos-i hwag-indoeeossseubnida.
EN The FDA can allow using vaccines before full approval
KO FDA는 최종 승인 이전이라도 백신 사용을 허용할 수 있습니다
Transliterasi FDAneun choejong seung-in ijeon-ilado baegsin sayong-eul heoyonghal su issseubnida
EN Zebra offers a wide variety of patented temperature monitoring and sensing devices, some of which are FDA-cleared medical devices
KO Zebra는 특허 받은 각종 온도 모니터링 및 감지 디바이스를 공급하며, 그중 일부는 FDA에서 허가한 의료 기기입니다
Transliterasi Zebraneun teugheo bad-eun gagjong ondo moniteoling mich gamji dibaiseuleul gong-geubhamyeo, geujung ilbuneun FDAeseo heogahan uilyo gigiibnida
| Basa inggris | Wong korea |
|---|---|
| zebra | zebra |
EN McKesson Packaging uses Cognex vision software for packaging and print quality inspection to keep up with FDA directives
KO McKesson Packaging에서는 FDA 기준을 준수하기 위한 패키지 작업 및 인쇄 품질 검사에 Cognex 비전 기술을 이용하고 있습니다
Transliterasi McKesson Packaging-eseoneun FDA gijun-eul junsuhagi wihan paekiji jag-eob mich inswae pumjil geomsa-e Cognex bijeon gisul-eul iyonghago issseubnida
EN ESPADA™ is an FDA-cleared medical device clinically proven to quickly & effectively treat acne-prone skin
KO ESPADA™는 트러블성 피부를 빠르고 효과적으로 관리하는 것으로 임상적으로 입증되어 FDA 승인을 받은 디바이스입니다
Transliterasi ESPADA™neun teuleobeulseong pibuleul ppaleugo hyogwajeog-eulo gwanlihaneun geos-eulo imsangjeog-eulo ibjeungdoeeo FDA seung-in-eul bad-eun dibaiseu-ibnida
EN TIBCO provides extensive support for enterprise governance in industries like finance, healthcare, insurance, manufacturing, and pharma, including ISO 9001, FDA 21 CFR Part 11 and GxP, GDPR, and CCPC.
KO ISO 9001, FDA 21 CFR Part 11 및 GxP, GDPR 및 CCPC를 포함한 금융, 의료, 보험, 제조 및 제약 등의 산업에서 엔터프라이즈 거버넌스를 광범위하게 지원합니다.
Transliterasi ISO 9001, FDA 21 CFR Part 11 mich GxP, GDPR mich CCPCleul pohamhan geum-yung, uilyo, boheom, jejo mich jeyag deung-ui san-eob-eseo enteopeulaijeu geobeoneonseuleul gwangbeom-wihage jiwonhabnida.
| Basa inggris | Wong korea |
|---|---|
| iso | iso |
| gdpr | gdpr |
EN Zebra offers a wide variety of patented temperature monitoring and sensing devices, some of which are FDA-cleared medical devices
KO Zebra는 특허 받은 각종 온도 모니터링 및 감지 디바이스를 공급하며, 그중 일부는 FDA에서 허가한 의료 기기입니다
Transliterasi Zebraneun teugheo bad-eun gagjong ondo moniteoling mich gamji dibaiseuleul gong-geubhamyeo, geujung ilbuneun FDAeseo heogahan uilyo gigiibnida
| Basa inggris | Wong korea |
|---|---|
| zebra | zebra |
EN Built-in technical controls combined with procedural controls ensure the security of your data, control access, and facilitate compliance as defined by US FDA 21 CFR Part 11, EU Annex 11 and similar national electronic record regulations
KO 절차 제어와 결합한 내장된 기술 제어가 데이터 보안을 보장하고 액세스를 제어하며 미국 FDA 21 CFR Part 11, EU Annex 11 및 이와 유사한 국가 전자 기록 규정의 규제 준수 지원
Transliterasi jeolcha jeeowa gyeolhabhan naejangdoen gisul jeeoga deiteo boan-eul bojanghago aegseseuleul jeeohamyeo migug FDA 21 CFR Part 11, EU Annex 11 mich iwa yusahan gugga jeonja gilog gyujeong-ui gyuje junsu jiwon
EN FDA cleared <Lunit INSIGHT MMG>
KO 후지필름-루닛 공동 개발 <CXR-AID> 일본 식약처 (PMDA) 인증
Transliterasi hujipilleum-lunis gongdong gaebal <CXR-AID> ilbon sig-yagcheo (PMDA) injeung
EN FDA cleared <Lunit INSIGHT CXR Triage>
KO 미국 식품의약국(FDA) 인가 <루닛 인사이트 MMG>
Transliterasi migug sigpum-uiyaggug(FDA) inga <lunis insaiteu MMG>
EN McKesson Packaging uses Cognex vision software for packaging and print quality inspection to keep up with FDA directives
KO McKesson Packaging에서는 FDA 기준을 준수하기 위한 패키지 작업 및 인쇄 품질 검사에 Cognex 비전 기술을 이용하고 있습니다
Transliterasi McKesson Packaging-eseoneun FDA gijun-eul junsuhagi wihan paekiji jag-eob mich inswae pumjil geomsa-e Cognex bijeon gisul-eul iyonghago issseubnida
EN This reduces risks associated with traditional testing and can even assist with FDA approval. It is a win-win situation that can increase safety and performance while simultaneously reducing development costs and time to market.
KO 따라서 기존 테스트와 관련된 위험을 줄이고 FDA 승인을 받는데도 도움이 될 수 있습니다. 안전성과 성능을 높이는 동시에 개발 비용과 출시 시간을 줄일 수 있는 윈-윈 전략입니다.
Transliterasi ttalaseo gijon teseuteuwa gwanlyeondoen wiheom-eul jul-igo FDA seung-in-eul badneundedo doum-i doel su issseubnida. anjeonseong-gwa seongneung-eul nop-ineun dongsie gaebal biyong-gwa chulsi sigan-eul jul-il su issneun win-win jeonlyag-ibnida.
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