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Regulatory and quality requirements for the design and development of Medical Device Software MasterClass
Regulatory and quality requirements for the design and development of Medical Device Software MasterClass
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Regulatory and quality requirements for the design and development of Medical Device Software MasterClass

12 Apr 2021 - 14 Apr 2021
Free Registration

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Regulatory and quality requirements for the design and development of Medical Device Software MasterClass

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Twenty-five years ago, software did not feature significantly in medical device legislation. Thirteen years ago it was added as a serious afterthought. As Europe moves to the new Medical Device Regulations, software is recognised throughout the General Safety and Performance Requirements. It has its own rules in classification, whether it is software as a medical device or software as the driver of a medical device. Software has come to the attention of the regulators as a serious source of risk and benefit. This sequence of seminars aims to help those involved in medical device software to understand intricacies of the regulatory burden and how early adoption of the solutions minimises both the costs and time to market.
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Entry Fees

Free Registration

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Event Frequency

One Time

Event Timings

(GMT+2:00) Budapest
09:00 AM - 05:00 PM (Apr 12, Apr 13, Apr 14) (General)

Organizer

GLC Europe

Global Leading Conferences (GLC) is a market leader in constructing industry focused events where business meets intelligence. We structure our events by investigating into market challenges and top issues that industries endure to render the m...

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M
MAMADOU SALIOU Barry
2021-03-12 11:55:06
Je souhaite recevoir des informations complémentaires pour inscription visiteurs et pour la demande de lettre d'inviation pour les demarches administratives.

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