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ENGLISH
ITALIANO
Corsi - Archivio 2024
13 dicembre 2024
Ricerca Clinica
ICH GCP (R3)
10 and 12 December 2024
Animal Health
/
Farmacovigilanza
Introduction to Veterinary Pharmacovigilance
10 December 2024
Ricerca Clinica
Master the New Swiss Clinical Trial Framework and its Interplay with the EU CTR - Similarities and Differences
28 November 2024
Farmacovigilanza
The “Global” Qualified Person Responsible for Pharmacovigilance (QPPV) Workshop
20 and 25 November 2024
Evidence Generation
/
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
Protocol Writing and Communication of Real World Evidence
19 and 21 November 2024
Farmacovigilanza
Mastering Benefit Risk Assessment in Pharmacovigilance
20 November 2024
Regolatorio
Decoding Electronic Product Information (ePI)
06, 13 and 20 November 2024
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
All You Need to Know to Understand Statistic if You are not a Statistician
11, 15 e 18 novembre 2024
Ricerca Clinica
Audit to Computer Systems
03 December 2024
Animal Health
/
Farmacovigilanza
Veterinary Pharmacovigilance Quality Management
13 e 15 novembre 2024
Ricerca Clinica
Condurre uno Studio Clinico Adempiendo alla Normativa GDPR: un Ponte fra Good Clinical Practices (GCP) e General Data Protection Regulation (GDPR)
05, 07, 12 e 14 novembre 2024
Farmacovigilanza
/
Ricerca Clinica
Safety Management e Farmacovigilanza
12 e 14 novembre 2024
Dispositivi Medici
/
Regolatorio
La Vigilanza Post Market per i Dispositivi Medici secondo MDR e FDA
12 and 14 November 2024
GMP Farmaceutico - Good Manufacturing Practices
Sterilization Validation
26 and 27 November 2024
Dispositivi Medici
/
Medical Affairs
/
Ricerca Clinica
Medical Reading
06, 08 e 13 novembre 2024
Regolatorio
Integratori Alimentari - Aspetti Tecnico-Regolatori e Panorama Normativo
27 November 2024
Animal Health
/
Regolatorio
Veterinary Marketing Authorisation Variation (MAV) in the EU
05 and 07 November 2024
Farmacovigilanza
/
Medical Affairs
/
Ricerca Clinica
Beyond PubMed
25 November 2024
GMP Farmaceutico - Good Manufacturing Practices
GMP Inspections: How to Be Ready?
30 October and 06 November 2024
GMP Farmaceutico - Good Manufacturing Practices
/
Regolatorio
Advanced Therapy Medicinal Product (ATMP): a Roadmap from Classification to Regulation and Manufacturing
19 and 21 November 2024
Farmacovigilanza
Pharmacovigilance Quality Management System (QMS)
19, 21, 26 and 28 November 2024
GMP Farmaceutico - Good Manufacturing Practices
Computer System Validation (CSV) and Assurance (CSA)
29 and 31 October 2024
GMP Farmaceutico - Good Manufacturing Practices
Cleaning Validation
29 and 30 October 2024
Dispositivi Medici
State of the Art Section for Medical Devices – Unpacking the Tips and Tricks of a Complex Document
30 October 2024
Animal Health
/
Regolatorio
Veterinary Marketing Authorisation Application (MAA) in the EU
29 October 2024
Dispositivi Medici
/
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
Writing Science for Lay Audiences
28 and 29 October 2024
Dispositivi Medici
Initiating the Development of Artificial Intelligence (AI) Medical Devices
21 e 24 ottobre 2024
Medical Affairs
/
Ricerca Clinica
Terapie Digitali (DTx): a che Punto Siamo?
22 and 23 October 2024
Animal Health
/
Farmacovigilanza
Veterinary Pharmacovigilance System
15 e 23 ottobre 2024
Medical Affairs
/
Regolatorio
/
Ricerca Clinica
Off-Label, Uso Compassionevole e Accesso Precoce (Early Access)
23 October 2024
Farmacovigilanza
/
Medical Writing
Pharmacovigilance Documents – Focus on Addendum to the Clinical Overview (AddCO) and Referrals
22 October 2024
Dispositivi Medici
What You Need to Know about Medical Device Software and Never Dared to Ask
04 novembre 2024
GMP Farmaceutico - Good Manufacturing Practices
La Compliance ai Requisiti GMP: Ruolo e Funzioni dell’Assicurazione Qualità
05 and 07 November 2024
Regolatorio
Marketing Authorization Application in EU, US and UK
17 October 2024
Farmacovigilanza
/
Medical Affairs
/
Medical Writing
/
Soft Skill
How to Create Effective Visuals for Better Communicating your Science
09 October and 16 October 2024
Farmacovigilanza
/
Medical Writing
Pharmacovigilance Documents – Focus on the Periodic Safety Update Report (PSUR)
15 and 16 October 2024
Dispositivi Medici
Medical Devices Periodic Safety Update Report (PSUR)
17 October 2024
GMP Farmaceutico - Good Manufacturing Practices
Human Error: the True Root Cause of a Deviation?
31 ottobre 2024
Dispositivi Medici
/
Farmacovigilanza
/
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
La Ricerca della Letteratura Scientifica: come Sfruttare le Risorse Gratuite in Rete
09 and 10 October 2024
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
Medical Writing Course: Improve your Writing & Reviewing Skills
23 and 24 October 2024
Medical Writing
/
Ricerca Clinica
Clinical Study Reports – a 360° Perspective
22 e 29 ottobre 2024
Regolatorio
Terapie Geniche e Terapie Cellulari
01 e 03 ottobre 2024
Regolatorio
Cosmetici - Aspetti Tecnico-Regolatori e Panorama Normativo
21 and 28 October 2024
GMP Farmaceutico - Good Manufacturing Practices
Biologics and Biosimilars Manufacturing
02 October 2024
Regolatorio
Electronic Submissions and Data Management in Regulatory Affairs
02 October 2024
Farmacovigilanza
/
Medical Writing
Pharmacovigilance Documents - Focus on the Risk Management Plan (RMP)
09 ottobre 2024
Regolatorio
Integratori Alimentari ed Advertising
15 and 17 October 2024
Regolatorio
The Basics of Regulatory Affairs for Cosmetic Products in US and Canada
15 October 2024
GMP Farmaceutico - Good Manufacturing Practices
Introduction to Aseptic Process Simulation (APS)
26 e 27 settembre 2024
Farmacovigilanza
/
GMP Farmaceutico - Good Manufacturing Practices
/
Ricerca Clinica
Buone Pratiche per la Gestione dei Documenti Cartacei e dei Dati Elettronici in Ambito GxP
25 e 26 settembre 2024
Dispositivi Medici
ISO 14155/2020 - Come Svolgere uno Studio Clinico con Dispositivi Medici
23 and 26 September 2024
Dispositivi Medici
/
Farmacovigilanza
/
Market Access Farmaceutico
/
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
Searching the Medical Literature
25 September 2024
Farmacovigilanza
/
Medical Writing
Pharmacovigilance Documents - Focus on Signal Management and Development Safety Update Reports (DSUR)
10 and 11 October 2024
Dispositivi Medici
/
Regolatorio
US FDA 101 - Fundamentals of Pre-market Submissions to CDRH
23 e 24 settembre 2024
Dispositivi Medici
/
Regolatorio
La Biocompatibilità e la Caratterizzazione Chimica: Dispositivi Medici Sicuri
STEP 2 : 10 and 17 October 2024
Evidence Generation
/
Medical Affairs
/
Ricerca Clinica
A Systematic Approach to Real World Evidence (RWE) Generation in Life Sciences - A 2 Step Intensive Course
24 e 26 settembre 2024
Dispositivi Medici
/
Farmacovigilanza
/
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
La Ricerca della Letteratura Scientifica: dal Quesito ai Risultati
16, 19 and 23 September 2024
Farmacovigilanza
/
Regolatorio
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
27 settembre 2024
Medical Affairs
/
Regolatorio
Codice Deontologico di Farmindustria e le Linee Guida per la Certificazione delle Attività Scientifiche: come applicarle in azienda
08 e 10 ottobre 2024
Regolatorio
Gestione della Proprietà Industriale - Il Brevetto per Tutelare le Invenzioni
20 settembre 2024
GMP Farmaceutico - Good Manufacturing Practices
ICH Q9 Quality Risk Management
19 e 20 settembre 2024
IVD - Dispositivi Medico Diagnostici In Vitro
/
Ricerca Clinica
La Conduzione di uno Studio Clinico con un Dispositivo Medico-Diagnostico in Vitro
18 e 19 settembre 2024
GMP Farmaceutico - Good Manufacturing Practices
EU GMP Annex 15 - La Qualifica e la Convalida nell'Industria Farmaceutica
17, 18 and 19 September 2024
Medical Writing
Tips and Tricks to Improve your Technical/Scientific Writing
18 September 2024
Farmacovigilanza
/
Medical Writing
Pharmacovigilance Documents - Basic Concepts and Definitions for Pharmacovigilance Writing
01 and 02 October 2024
GMP Farmaceutico - Good Manufacturing Practices
Process Validation
24, 26 settembre e 01 ottobre 2024
Market Access Farmaceutico
/
Medical Affairs
/
Regolatorio
Patient Support Program (PSP) e Patient Solution: Compiere una Scelta Strategica a Supporto del Paziente
16 September 2024
GMP Farmaceutico - Good Manufacturing Practices
Quality by Design
17 and 18 September 2024
Farmacovigilanza
Introduction to Pharmacovigilance
17 September 2024
Animal Health
/
Regolatorio
Good Distribution Practices (GDP) for Veterinary Medicinal Products
16 and 17 July 2024
Dispositivi Medici
/
Regolatorio
/
Ricerca Clinica
Good Distribution Practices of Medical Devices
25 e 27 giugno, 2 e 4 luglio 2024
Ricerca Clinica
Selezione e Convalida di Una Soluzione Cloud in Ambito GxP
02 July 2024
GMP Farmaceutico - Good Manufacturing Practices
Statistical Process Control for Pharmaceutical Manufacturing
28 giugno 2024
Ricerca Clinica
Qualifica dei Vendor nella Ricerca Clinica - Approfondimenti
18, 24 and 27 June 2024
Ricerca Clinica
/
Statistica e Data Management
A Practical Guide to Innovative Trial Design
26 giugno 2024
Regolatorio
Integratori Alimentari e Advertising: Applichiamo la Teoria alla Pratica
14 and 21 June 2024
Farmacovigilanza
The PSMF (Pharmacovigilance System Master File): from GVPs to Inspections
18 and 20 June 2024
Regolatorio
Fundamentals of European Cosmetics Regulatory Affairs
18 and 20 June 2024
Farmacovigilanza
Pharmacovigilance System: Audit & Inspection Readiness
19 and 20 June 2024
Dispositivi Medici
/
Regolatorio
Combination Products under the EU Medical Devices Regulation (MDR)
10 e 17 giugno 2024
Medical Affairs
Hospital Meeting: come Pianificare e Condurre una Riunione di Successo
10, 14 e 17 giugno 2024
Regolatorio
/
Ricerca Clinica
Computer System Validation (CSV) - GxP Process Owner and Quality Assurance: In or Out?
25 and 26 June 2024
Animal Health
/
Farmacovigilanza
Reporting Requirements in Veterinary Pharmacovigilance
02 and 03 July 2024
Dispositivi Medici
Labelling Requirements for Medical Devices
06, 07, 12 e 14 giugno 2024
Farmacovigilanza
Il Sistema di Qualità Applicato alla Farmacovigilanza
04, 06 e 11 giugno 2024
Farmacovigilanza
Signal Detection e Signal Management
12 e 13 giugno 2024
Medical Affairs
Il Patient Support Program (PSP) e la Transizione Digitale: Opportunità e Rischi
05 e 07 giugno 2024
Farmacovigilanza
La Gestione del Case Processing in Farmacovigilanza
04 e 06 giugno 2024
Ricerca Clinica
General Data Protection Regulation (GDPR), Ricerca Scientifica e Norme Locali
28 e 30 maggio 2024
Medical Affairs
Il Responsabile del Servizio Scientifico
21, 24 and 28 May 2024
Farmacovigilanza
/
Regolatorio
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
27 May 2024
Soft Skill
Oral Presentations
11 giugno 2024
GMP Farmaceutico - Good Manufacturing Practices
Le Good Calibration Practices (GCalP) negli Impianti Automatici di Produzione
23 e 24 maggio 2024
Medical Affairs
/
Soft Skill
La Gestione dell’Advisory Board nei Progetti Life Science
22 maggio 2024
Farmacovigilanza
/
Market Access Farmaceutico
/
Medical Affairs
/
Regolatorio
Patient Support Program (PSP) e Compliance: quali Normative Considerare?
22 maggio 2024
Regolatorio
Etichettatura degli Integratori Alimentari - Applichiamo la Normativa ad Esempi Reali
21 and 22 May 2024
Farmacovigilanza
Pharmacovigilance Agreements
14, 16 e 21 maggio 2024
Medical Affairs
Patient Advocacy ed Engagement nell’Azienda Farmaceutica
04 June 2024
Dispositivi Medici
/
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
How to Become a Successfully Published Author - Practical steps to make the publication process as smooth and as successful as possible
05 e 06 giugno 2024
Soft Skill
Comunicare con l'Intelligenza Relazionale
16 and 17 May 2024
Dispositivi Medici
/
IVD - Dispositivi Medico Diagnostici In Vitro
/
Regolatorio
Person Responsible for Regulatory Compliance (PRRC) - An MDR/IVDR Requirement
13, 15 and 16 May 2024
Dispositivi Medici
How to Write a Clinical Evaluation Plan and Report
07 e 09 maggio 2024
Regolatorio
La Pubblicità del Farmaco
08 maggio 2024
Medical Affairs
Progettare e Comunicare in Medical Affairs
15 e 16 maggio 2024
IVD - Dispositivi Medico Diagnostici In Vitro
La Sorveglianza Post-Market dei Dispositivi Diagnostici in Vitro
22 May 2024
Soft Skill
Beyond Slide Decks
29 April 2024
Dispositivi Medici
From Good to Excellent: The Summary of Safety and Clinical Performance (SSCP)
23 April 2024
Dispositivi Medici
Select the Ideal PMCF Strategy for a Medical Device
23 aprile 2024
Medical Affairs
Progettare un Patient Support Program (PSP): Configurazione del Processo e Strumenti
09 e 10 maggio 2024
GMP Farmaceutico - Good Manufacturing Practices
Agile Project Management: Gestire l’Innovazione nel Contesto della Produzione Farmaceutica
18 April 2024
Dispositivi Medici
/
IVD - Dispositivi Medico Diagnostici In Vitro
/
Medical Affairs
/
Regolatorio
Advertisement and Promotion Claims for Medical Devices
16 e 18 aprile 2024
Ricerca Clinica
Normativa della Ricerca Clinica tra Presente e Futuro
09 e 11 aprile 2024
Medical Affairs
Il Responsabile del Servizio Scientifico
10 and 11 April 2024
Medical Affairs
/
Medical Writing
/
Ricerca Clinica
Medical Writing Course: Improve your Writing & Reviewing Skills
10 aprile 2024
Medical Affairs
/
Regolatorio
/
Ricerca Clinica
I Radiofarmaci
03 e 05 aprile 2024
GMP Farmaceutico - Good Manufacturing Practices
Le Sfide della Produzione di un Investigational Medicinal Product (IMP)
03, 04 and 05 April 2024
Medical Affairs
/
Medical Writing
Clinical Study Protocols – Structure & Content
26 e 27 marzo 2024
GMP Farmaceutico - Good Manufacturing Practices
Annex 1 e Contamination Control Strategy
26 marzo 2024
Medical Affairs
/
Regolatorio
/
Ricerca Clinica
Il Consenso quale Base Giuridica per il Trattamento Dati nella Ricerca Clinico-Scientifica
20, 21 and 25 March 2024
Dispositivi Medici
How to Write a Clinical Evaluation Plan and Report
14, 19 e 21 marzo 2024
Medical Affairs
/
Ricerca Clinica
/
Statistica e Data Management
La Statistica Medica per Non Statistici
20 March 2024
Farmacovigilanza
“Attributability” in Pharmacovigilance: Still a Hot Topic
13 and 15 March 2024
Medical Affairs
The Next Generation of Medical Affairs: ChatGPT and Large Language Models (LLMs)
12 and 13 March 2024
Dispositivi Medici
Medical Devices Periodic Safety Update Report (PSUR)
06 and 07 March 2024
Dispositivi Medici
/
Regolatorio
Clinical Evaluation for Medical Devices
29 February and 01 March 2024
Dispositivi Medici
/
Regolatorio
Labelling Requirements for Medical Devices
TBD
Market Access Farmaceutico
Healthcare Modeling: Interventi per Migliorare Efficacia ed Efficienza delle Cure
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