Corsi

Medical Affairs / Ricerca Clinica

Il Futuro della Raccolta Dati nella Ricerca Clinica: Digital Endpoints e Digital Evidence

Farmacovigilanza

The “Global” Qualified Person Responsible for Pharmacovigilance (QPPV) Workshop

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 / Regolatorio

Advanced Therapy Medicinal Product (ATMP): a Roadmap from Classification to Regulation and Manufacturing

Ricerca Clinica

Audit to Computer Systems

20 October 2025

Regolatorio

Cosmetovigilance in the EU

21 October 2026

Cosmetici e Integratori / Farmacovigilanza / Regolatorio

Cosmetovigilance in the EU

Regolatorio

Food Supplement Regulations in the EU

29 September and 01 October 2026

Medical Writing / Ricerca Clinica

Writing Clinical Study Reports

25 and 29 September 2025

Medical Writing / Ricerca Clinica

Writing Clinical Study Reports

17 and 19 May 2027

Animal Health / Regolatorio

Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices

18 and 20 May 2026

Animal Health / Regolatorio

Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices

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 / Medical Affairs / 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 / Medical Affairs / Ricerca Clinica

A Systematic Approach to Real World Evidence (RWE) Generation in Life Sciences - a 2 step intensive course