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Pharmaceutical industry / Consumer protection law / Health / Medical equipment / Department of Health / Medicines and Healthcare products Regulatory Agency / Medical device / Medical Devices Directive / CE mark / Medicine / Clinical research / Technology


Regulation and Accreditation Proposal (RAMS) Sectorial Market Surveillance Programme for Medical Devices
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Document Date: 2013-06-24 07:24:31


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File Size: 102,53 KB

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City

Brussels / /

Company

Competent Authority / Vigilance Medical Device Expert Group / EU Medical Device Expert Group / Medical Expert Group / National Working Group / /

Continent

Europe / /

Country

United Kingdom / /

Event

Product Issues / Business Partnership / Product Recall / /

IndustryTerm

risk products / economic operator / Healthcare professionals / search warrant / to such products / individual device / dangerous consumer products / particular medical device / consumer medical devices / software updates / counter medical devices / compliant products / industrial products / unsafe devices / harmonisation legislation both before products / compliant devices / food / pharmaceutical and medical devices / /

Organization

MHRA / US Federal Reserve / European Commission / Market Surveillance Co-ordination Committee / Department for Business Innovation & Skills / national market surveillance authority / European Union / European parliament / Medicines and Healthcare products Regulatory Agency / UK Border Agency / UK’s Accreditation Service / Action Plan / and UK Government / UK Competent Authority / /

Position

General information support system / co-chair / representative / General / Secretary of State / /

Product

device / /

ProgrammingLanguage

EC / /

ProvinceOrState

California / /

SocialTag