SlideShares tagged with medical device regulations
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Medical Device Regulation (MDR) overview for Technion, May 25, 2021
Medical Device Regulation (MDR) overview for Technion, May 25, 20212y ago, 786 views
2y ago, 786 views -
mHealth Israel_MDR Bootcamp_Ulf Grundmann
mHealth Israel_MDR Bootcamp_Ulf Grundmann3y ago, 543 views
3y ago, 543 views -
Pakistan Medical Device regulatory process
Pakistan Medical Device regulatory process5y ago, 1,366 views
5y ago, 1,366 views -
Software as a Medical Device (SaMD) - IMDRF Definition and Categorisation
Software as a Medical Device (SaMD) - IMDRF Definition and Categorisation6y ago, 1,627 views
6y ago, 1,627 views -
The life sciences industry in 2018
The life sciences industry in 20186y ago, 1,109 views
6y ago, 1,109 views -
The European Medical Device Regulations - analysis of the final text
The European Medical Device Regulations - analysis of the final text7y ago, 1,511 views
7y ago, 1,511 views -
Laboratory, medical and device performance and validation following
Laboratory, medical and device performance and validation following7y ago, 28 views
7y ago, 28 views -
Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines
Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines7y ago, 25 views
7y ago, 25 viewsLike Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines SlideShare. Save Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines SlideShare. Share Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines SlideShare. -
Webinar: "The future of European Medical Device Regulations"
Webinar: "The future of European Medical Device Regulations"7y ago, 848 views
7y ago, 848 views -
Medical device regulations 510k
Medical device regulations 510k8y ago, 1,494 views
8y ago, 1,494 views -
EU Medical Devices Directive M5 Amendment 93 42 EEC Regulatory Update - BSI British Standards presentation
EU Medical Devices Directive M5 Amendment 93 42 EEC Regulatory Update - BSI British Standards presentation13y ago, 5,779 views
13y ago, 5,779 viewsLike EU Medical Devices Directive M5 Amendment 93 42 EEC Regulatory Update - BSI British Standards presentation SlideShare. Save EU Medical Devices Directive M5 Amendment 93 42 EEC Regulatory Update - BSI British Standards presentation SlideShare. Share EU Medical Devices Directive M5 Amendment 93 42 EEC Regulatory Update - BSI British Standards presentation SlideShare.
