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EU MDR 2017/745: Optimizing Clinical Evaluation Reports within the Medical Device Lifecycle
This Webinar is over| Date | Aug 7, 2018 |
| Time | 04:00 PM EDT |
| Cost | Free |
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Online
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Free webinar-online
In this webinar, NAMSA’s Manager of Medical Writing and Regulatory Services (EMEA), will examine the requirements listed in the MDR and MEDDEV 2.7/1 Rev 4, and discuss why device manufacturers shall not consider the CER a mandatory document for
NBs or authorities, but rather as a crucial tool for a smooth transition for MDR and beyond.
In this webinar, NAMSA’s Manager of Medical Writing and Regulatory Services (EMEA), will examine the requirements listed in the MDR and MEDDEV 2.7/1 Rev 4, and discuss why device manufacturers shall not consider the CER a mandatory document for
NBs or authorities, but rather as a crucial tool for a smooth transition for MDR and beyond.
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