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18 and 19 March 2021
Dispositivi Medici

How to Globally Register a Medical Device

English
17 and 18 March 2022
Dispositivi Medici / IVD - Dispositivi Medico Diagnostici In Vitro / Regolatorio

How to Globally Register a Medical Device

English
20 and 21 April 2023
Dispositivi Medici / IVD - Dispositivi Medico Diagnostici In Vitro / Regolatorio

How to Globally Register a Medical Device

English
NEW
25 and 26 March 2025
Ricerca Clinica

How to Implement the EU CTR in Sponsor Organisations to Ensure Compliance: A Practical Approach

English
23 and 25 March 2021
Dispositivi Medici

How to Write a Clinical Evaluation Plan

English
NEW
05 and 07 October 2021
Dispositivi Medici

How to Write a Clinical Evaluation Plan

English
01 and 03 March 2022
Dispositivi Medici

How to Write a Clinical Evaluation Plan

English
08, 15 and 17 November 2022
Dispositivi Medici

How to Write a Clinical Evaluation Plan and Report

English
14, 16 and 21 March 2023
Dispositivi Medici

How to Write a Clinical Evaluation Plan and Report

English
20, 21 and 25 March 2024
Dispositivi Medici

How to Write a Clinical Evaluation Plan and Report

English
13, 15 and 16 May 2024
Dispositivi Medici

How to Write a Clinical Evaluation Plan and Report

English
17, 18 and 22 September 2025
Dispositivi Medici

How to Write a Clinical Evaluation Plan and Report

English
13 and 15 April 2021
Dispositivi Medici

How to write a Clinical Evaluation Report from the MDR Perspective

English
19 and 20 October 2021
Dispositivi Medici

How to write a Clinical Evaluation Report from the MDR Perspective

English
12 and 14 April 2022
Dispositivi Medici

How to write a Clinical Evaluation Report from the MDR Perspective

English
NEW
17 October 2024
GMP Farmaceutico - Good Manufacturing Practices

Human Error: the True Root Cause of a Deviation?

English
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