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18 and 19 March 2021
Dispositivi Medici
How to Globally Register a Medical Device
17 and 18 March 2022
Dispositivi Medici
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IVD - Dispositivi Medico Diagnostici In Vitro
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Regolatorio
How to Globally Register a Medical Device
20 and 21 April 2023
Dispositivi Medici
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IVD - Dispositivi Medico Diagnostici In Vitro
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Regolatorio
How to Globally Register a Medical Device
NEW
25 and 26 March 2025
Ricerca Clinica
How to Implement the EU CTR in Sponsor Organisations to Ensure Compliance: A Practical Approach
23 and 25 March 2021
Dispositivi Medici
How to Write a Clinical Evaluation Plan
NEW
05 and 07 October 2021
Dispositivi Medici
How to Write a Clinical Evaluation Plan
01 and 03 March 2022
Dispositivi Medici
How to Write a Clinical Evaluation Plan
08, 15 and 17 November 2022
Dispositivi Medici
How to Write a Clinical Evaluation Plan and Report
14, 16 and 21 March 2023
Dispositivi Medici
How to Write a Clinical Evaluation Plan and Report
20, 21 and 25 March 2024
Dispositivi Medici
How to Write a Clinical Evaluation Plan and Report
13, 15 and 16 May 2024
Dispositivi Medici
How to Write a Clinical Evaluation Plan and Report
17, 18 and 22 September 2025
Dispositivi Medici
How to Write a Clinical Evaluation Plan and Report
13 and 15 April 2021
Dispositivi Medici
How to write a Clinical Evaluation Report from the MDR Perspective
19 and 20 October 2021
Dispositivi Medici
How to write a Clinical Evaluation Report from the MDR Perspective
12 and 14 April 2022
Dispositivi Medici
How to write a Clinical Evaluation Report from the MDR Perspective
NEW
17 October 2024
GMP Farmaceutico - Good Manufacturing Practices
Human Error: the True Root Cause of a Deviation?
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