GMP Richtlinien im Überblick und mit Durchblick |
https://www.gmp-navigator.com
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Good Manufacturing Procedure, Good Distribution Procedure, etc. |
FDA: 21 CFR part 820, Quality System Regulation |
https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H/part-820
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Ähnlich zu ISO 13485 |
FDA: Medical Devices; Quality System Regulation Amendments (Proposed Rule) Preliminary Regulatory Impact Analysis |
https://www.fda.gov/media/156552/download
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FDA: 21_CFR_part_807 Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices |
https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H/part-807
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Medical Device Single Audit Program - MDSAP |
https://www.fda.gov/media/87544/download
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Medical Device Regulation EU 2017/745 |
https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02017R0745-20200424
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FDA: 21 part 822 Post Market Surveilance |
https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H/part-822
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FDA - Medical Devices |
https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H
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EU - Eudamed2 - Info |
https://health.ec.europa.eu/medical-devices-sector/directives/market-surveillance-and-vigilance_en#which-information-is-stored-in-eudamed2
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EU - Medical Devices |
https://health.ec.europa.eu/medical-devices-topics-interest_de
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EU - Eudamed |
https://webgate.ec.europa.eu/eudamed/landing-page#/
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Beuth-Verlag für Normen |
https://www.beuth.de/de |
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Estonian Center for Standardisation |
https://www.evs.ee/en/ |
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