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Medical technology / Medical device / Global Harmonization Task Force / CE mark / Notified Body / Patient safety / Medical Devices Directive / European Medical Devices Industry Group / Medicines and Healthcare products Regulatory Agency / Medicine / Health / Medical equipment


Recast of the European Medical Devices Directives: an opportunity to reinforce patient safety ● Response to the public consultation on the recast of the Medical Devices Directives (1); deadline 2 July 2008 The Medicine
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Document Date: 2013-10-03 12:38:37


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Continent

Europe / /

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Facility

Hospital Pharmacists / /

IndustryTerm

medical implantable devices / invasive medical devices / healthcare professionals / healthcare-product medical devices / diagnostic devices / fact healthcare products / medical devices / active implantable medical devices / healthcare product / implantable and invasive devices / manufacturing practices / internal multidisciplinary expert / healthcare products / healthcare authority / cosmetic product / healthcare authorities / health technology products / healthcare / clinical devices / pharmaceutical quality / medicinal products / imported medical devices / /

MedicalTreatment

Innovative Therapies / /

Organization

Medical Device Committee / civil society / European Association of Hospital Pharmacists / Notified Bodies / International Society of Drug Bulletins / EMEA committee / Global Harmonization Task Force / European Commission / European Union / Welcomed Commission / /

Person

Catherine Hartmann / Teresa Alves / Maria Font / Antoine Vial / /

Position

reporter / /

ProgrammingLanguage

EC / /

URL

http /

SocialTag