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Ian Nicholls

Ian is a Director with extensive knowledge and experience in the management, development, implementation, and operation of processes and systems within the pharmaceutical and medical device industries. His skill set includes: • EU MDR 2017-745 / 21 CFR 820 / ISO 13485 / ISO 9001.

Confidentiality Protections

08/15/2022

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Member State Penalties

08/12/2022

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Trend Reporting: Monitoring the Market

08/01/2022

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What’s Included in the Post-Market Surveillance Plan?

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The Importance of Cooperation Among Authorities

07/01/2022

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EU MDR Competent Authorities

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Requirements Relating to Notified Bodies for EU MDR [Video]

04/01/2021

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The Difference Between UDI-DI and UDI-PI [Video]

02/11/2021

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Your 1 Minute Guide to Informed Consent

11/12/2020

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How to Conduct a Clinical Investigation

11/10/2020

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