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ENGLISH
ITALIANO
- Archive 2026
From 16 September to 22 October 2026
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents in the Life Cycle of a Medicinal Product
Dal 25 settembre al 21 novembre 2026
Clinical Research
Clinical Quality Assurance: un Ruolo Chiave nella Ricerca Clinica
06, 08 October 2026 | 13, 20 October 2026
Evidence Generation
/
Medical Affairs
/
Clinical Research
A Systematic Approach to Real World Evidence (RWE) Generation in Life Sciences - a 2 step intensive course
19 and 21 October 2026
Medical Affairs
/
Medical Writing
Hands-On Lab on AI Tools and Compliance with AI Act for Medical Affairs Professionals
20 and 21 October 2026
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
NEW COURSE
21 e 23 ottobre 2026
Medical Affairs
/
Regulatory
Dall’AIC alla Strategia Omnichannel di un Medicinale Senza Obbligo di Ricetta: Quadro Normativo, OTC Switch e Comunicazione
21 October 2026
Cosmetics and Food Supplements
/
Pharmacovigilance
/
Regulatory
Cosmetovigilance in the EU
22 October 2026
Animal Health
/
Pharmacovigilance
Veterinary Signal Detection
22 ottobre 2026
Pharmacovigilance
Italian Pharmacovigilance Day
27 and 29 October 2026
Pharmacovigilance
The PSMF (Pharmacovigilance System Master File): from GVPs to Inspections
27 ottobre e 03 novembre 2026
Medical Affairs
/
Regulatory
/
Clinical Research
Off-Label, Uso Compassionevole e Accesso Precoce (Early Access)
02 and 04 November 2026
Medical Device
/
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Beyond PubMed: Smarter Literature Monitoring for Life Sciences
02 and 03 November 2026
Medical Device
/
Regulatory
Pre-Market Submission of Medical Devices to the US FDA: Navigating the Pre-Sub and 510(k) Process
03, 05, 10 e 12 novembre 2026
Pharmacovigilance
/
Clinical Research
Safety Management e Farmacovigilanza
03, 05 e 10 novembre 2026
Cosmetics and Food Supplements
/
Regulatory
Integratori Alimentari - Aspetti Tecnico-Regolatori e Panorama Normativo
NEW COURSE
04 and 05 November 2026
Cosmetics and Food Supplements
/
Medical Device
/
Regulatory
Navigating Regulatory and Clinical Pathways for Cosmetic Products: A Practical Masterclass
NEW COURSE
09 novembre 2026
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Dispositivi Medici e Comunicazione Promozionale: Strategie, Compliance e Gestione del Rischio
NEW TRAINER
10, 11 and 12 November 2026
Medical Device
/
GMP (Good Manufacturing Practices)
/
Regulatory
End-to-End Ethylene Oxide Sterilization Validation for Medical Devices
10 e 12 novembre 2026
Medical Device
/
Regulatory
La Vigilanza Post Market per i Dispositivi Medici secondo MDR e FDA
11 November 2026
Pharmacovigilance
Nordic Pharmacovigilance Day
12 and 13 November 2026
Statistics and Data Management
European Statistical Forum
NEW COURSE
16 November 2026
Evidence Generation
/
Medical Affairs
/
Regulatory
/
Clinical Research
Patient Reported Outcomes (PROs) in Real World Evidence Generation
NEW COURSE
17 e 18 novembre 2026
Clinical Research
Data Governance e Sistemi Computerizzati negli Studi Clinici
17, 19 and 24 November 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
All you Need to Know to Understand Statistics if You are not a Statistician
18 and 25 November 2026
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on the Periodic Safety Update Report (PSUR)
18 and 19 November 2026
Pharmacovigilance
Mastering Benefit Risk Assessment in Pharmacovigilance
18, 19 e 24 novembre 2026
GMP (Good Manufacturing Practices)
ICH Q2 (R2): Le Novità nella Convalida dei Metodi Analitici
19 and 24 November 2026
Evidence Generation
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Protocol Writing and Communication of Real World Evidence
NEW COURSE
23 November 2026
Soft Skill
Leadership Essentials for Managers: Clarity, Competence and Impact
24 and 25 November 2026
Pharmacovigilance
Pharmacovigilance Agreements
NEW TRAINER
25 November 2026
Animal Health
/
Pharmacovigilance
Veterinary Pharmacovigilance Quality Management System (QMS)
26 e 27 novembre 2026
Market Access
Market Access: Anticipare le Sfide per Garantire l’Accesso ai Farmaci
16 ottobre 2026
Medical Affairs
/
Regulatory
/
Clinical Research
I Radiofarmaci
15 and 16 October 2026
Medical Device
MedDev Day
13 e 16 ottobre 2026
GMP (Good Manufacturing Practices)
Packaging Primario: Criteri Tecnici e Regolatori per Qualità, Sicurezza ed Efficacia del Prodotto Farmaceutico
13 and 15 October 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical and Scientific Reading
14 ottobre 2026
Clinical Research
ICH GCP (R3)
28 ottobre, 04 e 25 novembre 2026 e 10 febbraio 2027
Medical Affairs
Inside Out | MSL Lead
27 and 28 October 2026
GMP (Good Manufacturing Practices)
Ensuring Excellence in (Bio)pharmaceutical Cleaning Validation
05 e 09 ottobre 2026
Market Access
/
Medical Affairs
HTA Regulation e Accesso
07 e 09 ottobre 2026
Clinical Research
La Valutazione di Impatto della Protezione dei Dati (DPIA) nella Ricerca Clinico-Scientifica
07 and 08 October 2026
Medical Device
/
Medical Writing
State of the Art Section for Medical Devices – Unpacking the Tips and Tricks of a Complex Document
23, 28 e 30 ottobre 2026
Medical Device
/
Market Access
Il Market Access per i Dispositivi Medici
20, 22 and 27 October 2026
Soft Skill
Mastering Difficult Conversations in Healthcare
29 September and 01 October 2026
Medical Writing
/
Clinical Research
Writing Clinical Study Reports
29 settembre e 01 ottobre 2026
Cosmetics and Food Supplements
/
Regulatory
Cosmetici: Quadro Normativo Europeo e Requisiti Tecnico Regolatori Essenziali
30 September 2026
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on the Risk Management Plan (RMP)
22, 24 and 29 September 2026
Pharmacovigilance
Signal Detection and Signal Management
29 September 2026
Animal Health
/
Pharmacovigilance
Veterinary Signal Management
15 October 2026
Medical Affairs
/
Medical Writing
/
Soft Skill
How to Create Effective Visuals for Better Communicating your Science
28 September 2026
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
12 ottobre 2026
Cosmetics and Food Supplements
/
Regulatory
Etichettatura degli Integratori Alimentari
23 e 25 settembre 2026
Pharmacovigilance
/
GMP (Good Manufacturing Practices)
/
Clinical Research
Buone Pratiche per la Gestione dei Documenti Cartacei e dei Dati Elettronici in Ambito GxP
23 e 24 settembre 2026
Medical Device
Studi Clinici con Dispositivi Medici secondo ISO 14155/2026
23 and 24 September 2026
Medical Device
Labelling Requirements for Medical Devices
23 e 24 settembre 2026
Soft Skill
Comunicare Efficacemente con gli Operatori della Salute - Tecniche, Strumenti e Assertività per Dialogare al Meglio con Medici, Farmacisti e Operatori Sanitari
22 e 24 settembre 2026
Medical Device
/
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Ricerca della Letteratura Scientifica: dal Quesito ai Risultati
06, 13, 20 e 27 ottobre 2026
Pharmacovigilance
Inside Out | Pharmacovigilance Leadership
23 September 2026
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on Signal Management and Development Safety Update Reports (DSUR)
21 e 22 Settembre 2026
GMP (Good Manufacturing Practices)
EU GMP Annex 15 - La Qualifica e la Convalida nell'Industria Farmaceutica
22 settembre 2026
Medical Device
/
Evidence Generation
/
Medical Affairs
Progettare e Comunicare in Medical Affairs
07 and 08 October 2026
Medical Device
/
Regulatory
Combination Products under the EU Medical Devices Regulation (MDR)
16, 17 and 21 September 2026
Medical Device
How to Write a Clinical Evaluation Plan and Report
06 e 09 ottobre 2026
Medical Affairs
/
Regulatory
La Compliance che Genera Valore: l’Evoluzione del Ruolo nel Settore Farmaceutico
17 September 2026
Pharmacovigilance
German Pharmacovigilance Day
15 e 17 settembre 2026
Clinical Research
Norme, Novità e Futuro della Ricerca Clinica: Cosa Devi Sapere per Essere Compliant
30 settembre, 14 e 28 ottobre, 11 novembre 2026
Market Access
Inside Out | Market Access Excellence
30 settembre e 02 ottobre 2026
GMP (Good Manufacturing Practices)
ICH Q9 (R1) - Quality Risk Management: Gestire il Rischio per Governare la Qualità
07 e 08 ottobre 2026
Soft Skill
Comunicare con l'Intelligenza Relazionale
30 settembre e 02 ottobre 2026
Medical Affairs
Patient Solution: Trasformare Insight in Valore Reale per Pazienti e Organizzazioni
28 September and 01 October 2026
Soft Skill
Clinical Training Design: A Framework for Consistent, High-Value Clinical Education
16 and 17 September 2026
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
MDR/IVDR Requirement: The Person Responsible for Regulatory Compliance (PRRC)
16 September 2026
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Basic Concepts and Definitions for Pharmacovigilance Writing
17 e 18 settembre 2026
Medical Affairs
/
Soft Skill
La Gestione dell’Advisory Board nei Progetti Life Science
07 and 09 July 2026
Medical Device
/
GMP (Good Manufacturing Practices)
/
Regulatory
/
Clinical Research
Good Distribution Practices (GDP) for Medicines and Medical Devices
09 July 2026
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
02 July 2026
GMP (Good Manufacturing Practices)
Human Error: the True Root Cause of a Deviation?
01 July 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Writing Science for Lay Audiences
30 June 2026
Pharmacovigilance
/
Medical Writing
Narrative Writing in Pharmacovigilance - Ensuring Clarity, Consistency, and Regulatory Readiness in Line with ICH E2D/E2B(R3) and GVP Principles
25 giugno 2026
Clinical Research
Qualifica dei Vendor nella Ricerca Clinica - Approfondimenti
22, 23 and 24 June 2026
Clinical Research
/
Statistics and Data Management
A Practical Guide to Innovative Trial Design
22 June 2026
Cosmetics and Food Supplements
/
Regulatory
Food Supplement Regulations in the EU
17 e 19 giugno 2026
Regulatory
La Pubblicità del Farmaco
18 June 2026
Medical Affairs
/
Medical Writing
/
Clinical Research
/
Soft Skill
Presenting Science with Confidence: High-Impact Oral Presentations for Scientific and Medical Audiences
16 and 18 June 2026
Pharmacovigilance
Pharmacovigilance System: Audit & Inspection Readiness
10 e 17 giugno 2026
Medical Affairs
Come Pianificare e Condurre Hospital Meeting che Lasciano il Segno
09, 11 e 16 giugno 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Statistica Medica per Non Statistici
08, 12 e 15 giugno 2026
Regulatory
/
Clinical Research
Computer System Validation (CSV) - GxP Process Owner and Quality Assurance: In or Out?
23 and 25 June 2026
Medical Affairs
From AI Adoption to AI Responsibility - Understanding, Governing and Trusting AI in Life Sciences
09 e 11 giugno 2026
Pharmacovigilance
La Gestione del Case Processing in Farmacovigilanza
24 and 25 June 2026
Medical Device
/
Regulatory
Clinical Evaluation for Medical Devices
23, 24 and 25 June 2026
Medical Writing
Tips and Tricks to Improve your Technical/Scientific Writing
04 June 2026
Regulatory
Electronic Submissions and Data Management in Regulatory Affairs
27 e 29 maggio 2026
Pharmacovigilance
/
Medical Affairs
/
Regulatory
Patient Support Program: Progettazione, Compliance e Gestione Operativa
27 May 2026
Animal Health
/
Pharmacovigilance
Veterinary Pharmacovigilance System: From Compliance to Safety Excellence
18, 20 and 25 May 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Mastering Clinical Study Protocols: Practical Skills for Clinical Study Design
20 e 22 maggio 2026
GMP (Good Manufacturing Practices)
ICH Q14: Lo Sviluppo di Metodi Analitici
18 and 20 May 2026
Animal Health
/
Regulatory
Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices
12, 14 e 19 maggio 2026
Medical Affairs
Patient Advocacy ed Engagement in Ambito Farmaceutico ed Healthcare
12 May 2026
Medical Writing
/
Soft Skill
From Data to Impact: Don’t Let Bad Slides Ruin Good Science!
12 May 2026
Pharmacovigilance
/
Regulatory
Advanced Safety Management in Clinical Trials under CTR 536/2014
26 e 28 maggio 2026
GMP (Good Manufacturing Practices)
Gestione Efficace delle Deviazioni in Ambito GMP
26 e 27 maggio 2026
Medical Device
/
Regulatory
I Combination Products ai Sensi del Regolamento UE sui Dispositivi Medici (MDR)
05 and 07 May 2026
Cosmetics and Food Supplements
/
Regulatory
Global Cosmetic Compliance Made Simple
07 and 08 May 2026
Pharmacovigilance
Pharmacovigilance Agreements
06 May 2026
Pharmacovigilance
Effective Management of SAE/SUSAR Reporting and CIOMS Forms
19, 20 and 21 May 2026
Medical Affairs
/
Medical Writing
Writing Articles for Peer-Reviewed Journals: Turn Your Research into Published Results
30 aprile 2026
GMP (Good Manufacturing Practices)
Quality Agreement tra Officine, Clienti e Fornitori: dalla Teoria alla Pratica per Garantire Qualità e Conformità
13 e 15 maggio 2026
Medical Affairs
/
Medical Writing
Strumenti di Intelligenza Artificiale e Conformità all’AI Act per Professionisti del Medical Affair: Esercizi ed Esempi Pratici
21 e 23 aprile 2026
Cosmetics and Food Supplements
/
Regulatory
Integratori Alimentari e Pubblicità: Normativa, Rischi e Strategie di Conformità
21 and 23 April 2026
Regulatory
Fast-Track Your Marketing Authorization Application (MAA): Navigate EU, UK & US Regulatory Pathways with Confidence
Dal 27 febbraio al 22 aprile 2026
Medical Affairs
Medical Affairs Essentials
22 aprile 2026
Clinical Research
Deviazioni negli Studi Clinici: Riconoscerle, Gestirle, Prevenirle
22 April 2026
Medical Device
Summary of Safety and Clinical Performance (SSCP)
07 maggio 2026
Evidence Generation
/
Medical Affairs
/
Clinical Research
Generare Real World Evidence (RWE) con Metodi Osservazionali
15 e 17 aprile 2026
Medical Affairs
Il Responsabile del Servizio Scientifico
08, 10, 15 e 17 aprile 2026
Pharmacovigilance
Il Sistema di Qualità Applicato alla Farmacovigilanza
16 April 2026
GMP (Good Manufacturing Practices)
Introduction to Aseptic Process Simulation (APS)
15 April 2026
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
09 and 14 April 2026
Animal Health
/
Pharmacovigilance
Introduction to Veterinary Pharmacovigilance
14 e 15 aprile 2026
Clinical Research
Protezione dei dati personali (GDPR) e Ricerca Scientifica
14 April 2026
Medical Device
PMCF under MDR: Turning Compliance into Clinical Value
08 e 09 aprile 2026
GMP (Good Manufacturing Practices)
Annex 1 e Contamination Control Strategy
01 e 02 aprile 2026
Regulatory
Terapie Geniche e Terapie Cellulari
31 marzo e 01 aprile 2026
GMP (Good Manufacturing Practices)
Serializzazione e Tracciatura dei Farmaci
26 and 27 March 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
25 March 2026
Pharmacovigilance
Attributability and Causality in Pharmacovigilance: Still a Hot Topic
24 March 2026
Clinical Research
Master the New Swiss Clinical Trial Framework and its Interplay with the EU CTR - Similarities and Differences
18 e 19 marzo 2026
Medical Device
/
Regulatory
La Biocompatibilità e la Caratterizzazione Chimica: Dispositivi Medici Sicuri
19 March 2026
Pharmacovigilance
The “Global” Qualified Person Responsible for Pharmacovigilance (QPPV) Workshop
18 marzo 2026
Medical Affairs
/
Clinical Research
Il Consenso è davvero l’unica Base Giuridica per il Trattamento Dati nella Ricerca Clinico-Scientifica?
10, 12 e 17 marzo 2026
GMP (Good Manufacturing Practices)
La Qualifica dei Fornitori GMP
11 and 12 March 2026
Medical Device
Labelling Requirements for Medical Devices
09 March 2026
Animal Health
/
Pharmacovigilance
Veterinary QPPV Oversight
05 e 06 marzo 2026
Medical Affairs
/
Clinical Research
/
Soft Skill
Dalla Comunicazione Professionale alla Negoziazione
04 and 05 March 2026
Medical Device
/
Medical Writing
Mastering MDCG 2024-3: Comprehensive Training on Clinical Investigation Plans
25 and 26 February 2026
Medical Device
/
Regulatory
Clinical Evaluation for Medical Devices
TBD
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Searching the Medical Literature
TBD
Clinical Research
Selezione e Convalida di Una Soluzione Cloud in Ambito GxP
TBD
Regulatory
Decoding Electronic Product Information (ePI)
TBD
Regulatory
Mastering ISO IDMP: EU Implementation and Regulatory Impact
TBD
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on Addendum to the Clinical Overview (AddCO) and Referrals
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