6.2 Regulatory Requirement: 21 CFR Part 807 Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices
In: Biomedical Quality Auditor Handbook 2003; (2003)
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E-Book
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6.2 Regulatory Requirement: 21 CFR Part 807 Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices
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Autor/in / Beteiligte Person: | Bruce, Haggar |
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Quelle: | Biomedical Quality Auditor Handbook 2003; (2003) |
Veröffentlichung: | 2003 |
Medientyp: | E-Book |
ISBN: | 978-1-62198-041-4 (print) ; 978-0-87389-576-7 (print) |
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