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NEW COURSE
7 Ottobre 2025
Medical Affairs
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Ricerca Clinica
Il Futuro della Raccolta Dati nella Ricerca Clinica: Digital Endpoints e Digital Evidence
11 March 2027
Farmacovigilanza
The “Global†Qualified Person Responsible for Pharmacovigilance (QPPV) Workshop
19 March 2026
Farmacovigilanza
The “Global†Qualified Person Responsible for Pharmacovigilance (QPPV) Workshop
15 and 16 May 2025
Dispositivi Medici
Labelling Requirements for Medical Devices
13 and 18 November 2025
GMP Farmaceutico - Good Manufacturing Practices
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Regolatorio
Advanced Therapy Medicinal Product (ATMP): a Roadmap from Classification to Regulation and Manufacturing
TBD
Ricerca Clinica
Audit to Computer Systems
NEW COURSE
20 October 2025
Regolatorio
Cosmetovigilance in the EU
21 October 2026
Cosmetici e Integratori
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Farmacovigilanza
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Regolatorio
Cosmetovigilance in the EU
NEW COURSE
23 June 2025
Regolatorio
Food Supplement Regulations in the EU
29 September and 01 October 2026
Medical Writing
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Ricerca Clinica
Writing Clinical Study Reports
25 and 29 September 2025
Medical Writing
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Ricerca Clinica
Writing Clinical Study Reports
17 and 19 May 2027
Animal Health
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Regolatorio
Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices
18 and 20 May 2026
Animal Health
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Regolatorio
Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices
NEW COURSE
19 and 21 May 2025
Animal Health
/
Regolatorio
Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices
14, 21 October 2025 | 18, 27 November 2025
Evidence Generation
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Medical Affairs
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Ricerca Clinica
A Systematic Approach to Real World Evidence (RWE) Generation in Life Sciences - a 2 step intensive course
06, 08 October 2026 | 13, 20 October 2026
Evidence Generation
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Medical Affairs
/
Ricerca Clinica
A Systematic Approach to Real World Evidence (RWE) Generation in Life Sciences - a 2 step intensive course
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