In Vitro Diagnostic Medical Devices Evaluation Of Stability Of In Vitro Diagnostic Reagents
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Author : World Health Organization Publisher : World Health Organization Page : 34 pages File Size : 53,5 Mb Release : 2023-03-06 Category : Medical ISBN : 9789240057487
Author : World Health Organization Publisher : World Health Organization Page : 34 pages File Size : 51,7 Mb Release : 2023-10-02 Category : Medical ISBN : 9789240077751
Author : World Health Organization Publisher : World Health Organization Page : 35 pages File Size : 43,6 Mb Release : 2023-03-06 Category : Medical ISBN : 9789240057500
Author : World Health Organization Publisher : World Health Organization Page : 35 pages File Size : 46,7 Mb Release : 2023-11-23 Category : Medical ISBN : 9789240082939
Author : World Health Organization Publisher : World Health Organization Page : 31 pages File Size : 45,6 Mb Release : 2021-11-30 Category : Medical ISBN : 9789240039346
In Vitro Diagnostic Medical Devices. Information Supplied by the Manufacturer (Labelling). Terms, Definitions and General Requirements by British Standards Institute Staff Pdf
In Vitro Diagnostic Medical Devices. Information Supplied by the Manufacturer (Labelling). in Vitro Diagnostic Reagents for Professional Use by British Standards Institute Staff Pdf
Diagnosis (medical), Medical equipment, Product information, Instructions for use, Labels, Labelling (process), Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Containers, Health service personnel
In Vitro Diagnostic Medical Devices. Information Supplied by the Manufacturer with in Vitro Diagnostic Reagents for Staining in Biology by British Standards Institute Staff Pdf
Medical equipment, Medical laboratory equipment, Biological stains, Dyes, Chemical reagents, Diagnosis (medical), Biological analysis and testing, Reproducibility
Medical Devices and In Vitro Diagnostics by Christian Baumgartner,Johann Harer,Jörg Schröttner Pdf
This updatable reference work gives a comprehensive overview of all relevant regulatory information and requirements for manufacturers and distributors around medical and in-vitro diagnostic devices in Europe. These individual requirements are presented in a practice-oriented manner, providing the reader with a concrete guide to implementation with main focus on the EU medical device regulations, such as MDR 2017/745 and IVD-R 2017/746, and the relevant standards, such as the ISO 13485, ISO 14971, among others. This book offers a good balance of expert knowledge, empirical values and practice-proven methods. Not only it provides readers with a quick overview about the most important requirements in the medical device sector, yet it shows concrete and proven ways in which these requirements can be implemented in practice. It addresses medical manufacturing companies, professionals in development, production, and quality assurance departments, and technical and medical students who are preparing themselves for a professional career in the medical technlogy industries.
