Medical Devices and IVDs - 11 Angebote vergleichen

Lieferung aus: Schweiz, Download sofort lieferbar.
Market Access under the new EU Regulations - compact course for study, project and job, eBooks, eBook Download (EPUB), Are you fit for the new rules in Europe? The new EU regulations on medical devices and in vitro diagnostic medical devices (IVDs) are changing the rules of the game in this important area of health care. It is now necessary to adapt quickly to the new and more demanding rules on market access in Europe. This requires a thorough knowledge of the new rules for all those responsible and employed in the sector. A sound knowledge of the new EU regulations is also indispensable for the education, training and further education of students, and for staff in research and development, in regulatory affairs and quality management. For all those who are active and responsible in the field of medical technology, biomedical and clinical engineering, e-health and related fields. The new 3rd edition gives the latest stage of regulatory corrigenda, amendments and EU-target dates and reflects the latest Guidance documents of EU on this. Don't be late: those that fail to prepare - prepare to fail! 336 pages; 38 Fig., 23 Tab.

Lieferung aus: Niederlande, Direct beschikbaar.
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Are you fit for the new rules in Europe? The new EU regulations on medical devices and in vitro diagnostic medical devices (IVDs) are changing the rules of the game in this important area of health care. It is now necessary to adapt quickly to the new and more demanding rules on market access in Europe. This requires a thorough knowledge of the new rules for all those responsible and employed in the sector. A sound knowledge of the new EU regulations is also indispensable for the education, training and further education of students, and for staff in research and development, in regulatory affairs and quality management. For all those who are active and responsible in the field of medical technology, biomedical and clinical engineering, e-health and related fields. The new 3rd edition gives the latest stage of regulatory corrigenda, amendments and EU-target dates and reflects the latest Guidance documents of EU on this. Don't be late: those that fail to prepare - prepare to fail! 336 pages; 38 Fig., 23 Tab. Are you fit for the new rules in Europe? The new EU regulations on medical devices and in vitro diagnostic medical devices (IVDs) are changing the rules of the game in this important area of health care. It is now necessary to adapt quickly to the new and more demanding rules on market access in Europe. This requires a thorough knowledge of the new rules for all those responsible and employed in the sector. A sound knowledge of the new EU regulations is also indispensable for the education, training and further education of students, and for staff in research and development, in regulatory affairs and quality management. For all those who are active and responsible in the field of medical technology, biomedical and clinical engineering, e-health and related fields. The new 3rd edition gives the latest stage of regulatory corrigenda, amendments and EU-target dates and reflects the latest Guidance documents of EU on this. Don't be late: those that fail to prepare - prepare to fail! 336 pages; 38 Fig., 23 Tab. Inhoud:Taal: Engels;Bindwijze: E-book;Druk: 3;Verschijningsdatum: juni 2021;Ebook formaat: Adobe ePub;Illustraties: Nee; Betrokkenen:Auteur(s): Wolfgang Ecker;Uitgever: Books On Demand; Lees mogelijkheden:Lees dit ebook op: Android (smartphone en tablet) | Kobo e-reader | Overige e-reader | Desktop (Mac en Windows) | iOS (smartphone en tablet) | Windows (smartphone en tablet);Ebook formaat: Adobe ePub; EAN: Overige kenmerken:Studieboek: Ja; Engels | Druk: 3 | E-book | 9783753452500.

Lieferung aus: Deutschland, Versandkostenfrei innerhalb von Deutschland.
The new EU regulations on medical devices and in vitro diagnostic medical devices (IVDs) are changing the rules of the game in this important area of health care. It is now necessary to make use of the transitional periods and adapt quickly to the new and more demanding rules on market access. This requires a thorough knowledge of the new rules for all those responsible and employed in the sector. A sound knowledge of the new EU regulations is also indispensable for the education, training and The new EU regulations on medical devices and in vitro diagnostic medical devices (IVDs) are changing the rules of the game in this important area of health care. It is now necessary to make use of the transitional periods and adapt quickly to the new and more demanding rules on market access. This requires a thorough knowledge of the new rules for all those responsible and employed in the sector. A sound knowledge of the new EU regulations is also indispensable for the education, training and further education of students, and staff in research and development, regulatory affairs and quality management, active in the field of medical technology, biomedical and clinical engineering, e-health and related fields. 240 pages; 35 Fig., 18 Tab. Sofort per Download lieferbar Lieferzeit 1-2 Werktage.

Lieferung aus: Deutschland, Versandkostenfrei.
Medical Devices and IVDs: The new EU regulations on medical devices and in vitro diagnostic medical devices (IVDs) are changing the rules of the game in this important area of health care. It is now necessary to make use of the transitional periods and adapt quickly to the new and more demanding rules on market access. This requires a thorough knowledge of the new rules for all those responsible and employed in the sector. A sound knowledge of the new EU regulations is also indispensable for the education, training and further education of students, and staff in research and development, regulatory affairs and quality management, active in the field of medical technology, biomedical and clinical engineering, e-health and related fields.240 pages 35 Fig., 18 Tab. Englisch, Ebook.

Lieferung aus: Deutschland, E-Book zum Download, Versandkostenfrei.
The new EU regulations on medical devices and in vitro diagnostic medical devices (IVDs) are changing the rules of the game in this important area of health care. It is now necessary to make use of the transitional periods and adapt quickly to the new and more demanding rules on market access. This requires a thorough knowledge of the new rules for all those responsible and employed in the sector. A sound knowledge of the new EU regulations is also indispensable for the education, training and further education of students, and staff in research and development, regulatory affairs and quality management, active in the field of medical technology, biomedical and clinical engineering, e-health and related fields. 240 pages; 35 Fig., 18 Tab. Kindle Edition, Ausgabe: 1, Format: Kindle eBook, Label: Books on Demand, Books on Demand, Produktgruppe: eBooks, Publiziert: 2019-01-25, Freigegeben: 2019-01-25, Studio: Books on Demand.

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Lieferung aus: Deutschland, Versandkostenfrei innerhalb von Deutschland.
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