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ISO 13485:2016 Reviews

Thennarasu s, 15 Dec 2023

Device classification , Rules can be added. Automation related GMP contents were missing. Risk management standard contents was high level

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Krishna S, 27 Nov 2023

Good

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Agne A, 27 Nov 2023

N/A

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Roisin K, 27 Nov 2023

Very good course, really enjoyable and would highly recommend this course for anyone looking to get an good understanding of the Medical Device industry and in particular the regulations and QMS importance of Medical Device Manufacturing.

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Richard B, 25 Jul 2023

Very well run course, Anne Marie was very helpful in answering all of our questions.

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Vedika K, 25 Jul 2023

Very informative,

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Eoin R, 23 May 2023

Excellent as always

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Maria V, 19 Apr 2023

Kevina, I am privileged to attend this training. I look forward to applying the skills I gained in my career and profession.

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Cian M, 18 Apr 2023

Good content and material, well delivered and engaging, majority is very applicable to role.

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Rebecca M, 18 Apr 2023

A pretty intense course but Kevina made it rather enjoyable. Learned soo much about where my role fits.

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