Six Key New Commission Documents Relating To EU Directives And New Regulations
Six Key New Commission Documents Relating To EU Directives And New Regulations
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To help companies respond and adapt the processes they may have in place as rapid EU regulatory activity continues, Medtech Insight summarizes the six documents that have recently appeared on the European Commission’s medtech website.
Author: Informa Pharma Intelligence
Publisher: Medtech
- Description
The European Commission has published a host of information that is relevant to those preparing to comply with the EU’s Medical Device Regulation which fully applies from 26 May 2020 as well as relevant information about Medical Device Directives. Medtech Insight shares summaries of the six key documents so companies can be ready to respond.
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