Corsi

NEW
03, 04 e 10 giugno 2025
GMP Farmaceutico - Good Manufacturing Practices

ICH Q2 (R2): Le Novità nella Convalida dei Metodi Analitici

Italiano
TBD
Medical Affairs / Regolatorio

Codice Deontologico di Farmindustria e le Linee Guida per la Certificazione delle Attività di Informazione Scientifica: come applicarle in Azienda

Italiano
08 and 09 October 2025
Dispositivi Medici / Medical Writing

State of the Art Section for Medical Devices – Unpacking the Tips and Tricks of a Complex Document

English
09, 13 e 16 giugno 2025
Regolatorio / Ricerca Clinica

Computer System Validation (CSV) - GxP Process Owner and Quality Assurance: In or Out?

Italiano
22 e 23 settembre 2025
GMP Farmaceutico - Good Manufacturing Practices

EU GMP Annex 15 - La Qualifica e la Convalida nell'Industria Farmaceutica

Italiano
21 and 23 April 2026
Regolatorio

Fast-Track Your Marketing Authorization Application (MAA): Navigate EU, UK & US Regulatory Pathways with Confidence

English
NEW
14 and 15 April 2025
Regolatorio

Mastering the Essentials of Marketing Authorisation Application (MAA): A Path to Regulatory Success in the EU, UK and US

English
NEW
TBD
GMP Farmaceutico - Good Manufacturing Practices

Biologics and Biosimilars Manufacturing

English
NEW
10 and 11 November 2025
Dispositivi Medici / Regolatorio

Pre-Market Submission of Medical Devices to the US FDA: Navigating the Pre-Sub and 510(k) Process

English
NEW
10 December 2024
Ricerca Clinica

Master the New Swiss Clinical Trial Framework and its Interplay with the EU CTR - Similarities and Differences

English
NEW
21 maggio 2025
GMP Farmaceutico - Good Manufacturing Practices

ICH Q14: Lo Sviluppo di Metodi Analitici

Italiano
NEW
21 e 23 aprile 2026
Regolatorio

Integratori Alimentari e Pubblicità: Normativa, Rischi e Strategie di Conformità

Italiano
23, 24 and 25 June 2026
Medical Writing

Tips and Tricks to Improve your Technical/Scientific Writing

English
24, 25 and 26 June 2025
Medical Writing

Tips and Tricks to Improve your Technical/Scientific Writing

English
NEW
23, 25 and 30 September 2025
Farmacovigilanza

Signal Detection and Signal Management

English
09 and 10 October 2025
Dispositivi Medici / Regolatorio

Combination Products under the EU Medical Devices Regulation (MDR)

English