Webinar
Medical Devices

MDR Rule 14 Devices

Conformity assessment process and documentation requirements for submissions

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This webinar:

Device and Drug Combinations in EU.
Introduction to BSI Medicinal team.
MDCG 2020-12 - MDR Conformity Assessment Process.
Competent Authority Assessment & Documentation Requirements.

Speakers

Hear from the experts in this webinar

Speaker

Theresa Jeary

Global Head - Medicinal & Biologics, BSI

Insights & Media

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Informatie en media

EU MDR – Post Market Clinical Follow-Up

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Annex XVI - Devices Without an Intended Medical Purpose

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Using Standards to Demonstrate Conformity

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Unlocking the Potential of Consumer Wearables in Healthcare

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Medical Device Lifetime - Assisting manufacturers

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Symbols & Details Required for Medical Devices & IVDs

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