- Archivio 2024

Dal 04 ottobre al 13 dicembre 2024

Medical Affairs

Medical Affairs: Prepararsi alle Sfide Future di un Ruolo Complesso

13 dicembre 2024

Ricerca Clinica

ICH GCP (R3)

10 and 12 December 2024

Animal Health / Farmacovigilanza

Introduction to Veterinary Pharmacovigilance

03 December 2024

Animal Health / Farmacovigilanza

Veterinary Pharmacovigilance Quality Management

19, 21, 26 and 28 November 2024

GMP Farmaceutico - Good Manufacturing Practices

Computer System Validation (CSV) and Assurance (CSA)

28 November 2024

Farmacovigilanza

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

27 November 2024

Animal Health / Regolatorio

Veterinary Marketing Authorisation Variation (MAV) in the EU

26 and 27 November 2024

Dispositivi Medici / Medical Affairs / Ricerca Clinica

Medical Reading

20 and 25 November 2024

Evidence Generation / Medical Affairs / Medical Writing / Ricerca Clinica

Protocol Writing and Communication of Real World Evidence

25 November 2024

GMP Farmaceutico - Good Manufacturing Practices

GMP Inspections: How to Be Ready?

dal 27 settembre al 23 novembre 2024

Ricerca Clinica

Clinical Quality Assurance: un Ruolo Chiave nella Ricerca Clinica

19 and 21 November 2024

Farmacovigilanza

Mastering Benefit Risk Assessment in Pharmacovigilance

19 and 21 November 2024

Farmacovigilanza

Pharmacovigilance Quality Management System (QMS)

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

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)

12 and 14 November 2024

GMP Farmaceutico - Good Manufacturing Practices

Sterilization Validation

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

06, 08 e 13 novembre 2024

Regolatorio

Integratori Alimentari - Aspetti Tecnico-Regolatori e Panorama Normativo

13 November 2024

Farmacovigilanza

Nordic Pharmacovigilance Day

05 and 07 November 2024

Regolatorio

Marketing Authorization Application in EU, US and UK

05 and 07 November 2024

Farmacovigilanza / Medical Affairs / Ricerca Clinica

Beyond PubMed

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

04 novembre 2024

GMP Farmaceutico - Good Manufacturing Practices

La Compliance ai Requisiti GMP: Ruolo e Funzioni dell’Assicurazione Qualità

31 ottobre 2024

Dispositivi Medici / Farmacovigilanza / Medical Affairs / Medical Writing / Ricerca Clinica

La Ricerca della Letteratura Scientifica: come Sfruttare le Risorse Gratuite in Rete

29 and 31 October 2024

GMP Farmaceutico - Good Manufacturing Practices

Cleaning Validation

30 October 2024

Animal Health / Regolatorio

Veterinary Marketing Authorisation Application (MAA) in the EU

22 e 29 ottobre 2024

Regolatorio

Terapie Geniche e Terapie Cellulari

28 and 29 October 2024

Dispositivi Medici

Initiating the Development of Artificial Intelligence (AI) Medical Devices

29 October 2024

Dispositivi Medici / Medical Affairs / Medical Writing / Ricerca Clinica

Writing Science for Lay Audiences

21 e 24 ottobre 2024

Medical Affairs / Ricerca Clinica

Terapie Digitali (DTx): a che Punto Siamo?

23 and 24 October 2024

Medical Writing / Ricerca Clinica

Clinical Study Reports – a 360° Perspective

From 18 September to 23 October 2024

Farmacovigilanza / Medical Writing

Pharmacovigilance Documents in the Life Cycle of a Medicinal Product

23 October 2024

Farmacovigilanza / Medical Writing

Pharmacovigilance Documents – Focus on Addendum to the Clinical Overview (AddCO) and Referrals

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)

22 October 2024

Dispositivi Medici

What You Need to Know about Medical Device Software and Never Dared to Ask

23 Ottobre 2024

Farmacovigilanza

Italian Pharmacovigilance Day

17 October 2024

Farmacovigilanza / Medical Affairs / Medical Writing / Soft Skill

How to Create Effective Visuals for Better Communicating your Science

17 October 2024

GMP Farmaceutico - Good Manufacturing Practices

Human Error: the True Root Cause of a Deviation?

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)

10 and 11 October 2024

Dispositivi Medici

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

09 and 10 October 2024

Medical Affairs / Medical Writing / Ricerca Clinica

Medical Writing Course: Improve your Writing & Reviewing Skills

07 and 08 October 2024

Dispositivi Medici

MedDev Day

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

Farmacovigilanza / Medical Writing

Pharmacovigilance Documents - Focus on the Risk Management Plan (RMP)

02 October 2024

Regolatorio

Electronic Submissions and Data Management in Regulatory Affairs

15 and 17 October 2024

Regolatorio

The Basics of Regulatory Affairs for Cosmetic Products in US and Canada

09 ottobre 2024

Regolatorio

Integratori Alimentari ed Advertising

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

23 and 26 September 2024

Dispositivi Medici / Farmacovigilanza / Market Access Farmaceutico / Medical Affairs / Medical Writing / Ricerca Clinica

Searching the Medical Literature

25 e 26 settembre 2024

Dispositivi Medici

ISO 14155/2020 - Come Svolgere uno Studio Clinico con Dispositivi Medici

25 September 2024

Farmacovigilanza / Medical Writing

Pharmacovigilance Documents - Focus on Signal Management and Development Safety Update Reports (DSUR)

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

10 and 11 October 2024

Dispositivi Medici / Regolatorio

US FDA 101 - Fundamentals of Pre-market Submissions to CDRH

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

17, 18 and 19 September 2024

Medical Writing

Tips and Tricks to Improve your Technical/Scientific Writing

18 e 19 settembre 2024

GMP Farmaceutico - Good Manufacturing Practices

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

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

17 September 2024

Farmacovigilanza

German Pharmacovigilance Day

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

17 and 18 September 2024

Farmacovigilanza

Introduction to Pharmacovigilance

17 September 2024

Animal Health / Regolatorio

Good Distribution Practices (GDP) for Veterinary Medicinal Products

16 September 2024

GMP Farmaceutico - Good Manufacturing Practices

Quality by Design

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

GMP Farmaceutico - Good Manufacturing Practices

Statistical Process Control for Pharmaceutical Manufacturing

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

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, 14 e 17 giugno 2024

Regolatorio / Ricerca Clinica

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

10 e 17 giugno 2024

Medical Affairs

Hospital Meeting: come Pianificare e Condurre una Riunione di Successo

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

Oral Presentations

21, 24 and 28 May 2024

Farmacovigilanza / Regolatorio

Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014

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

Regolatorio

Etichettatura degli Integratori Alimentari - Applichiamo la Normativa ad Esempi Reali

Farmacovigilanza / Market Access Farmaceutico / Medical Affairs / Regolatorio

Patient Support Program (PSP) e Compliance: quali Normative Considerare?

21 and 22 May 2024

Farmacovigilanza

Pharmacovigilance Agreements

14, 16 e 21 maggio 2024

Medical Affairs

Patient Advocacy ed Engagement nell’Azienda Farmaceutica

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

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

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

Beyond Slide Decks

Dispositivi Medici

From Good to Excellent: The Summary of Safety and Clinical Performance (SSCP)

Medical Affairs

Progettare un Patient Support Program (PSP): Configurazione del Processo e Strumenti

Dispositivi Medici

Select the Ideal PMCF Strategy for a Medical Device

09 e 10 maggio 2024

GMP Farmaceutico - Good Manufacturing Practices

Agile Project Management: Gestire l’Innovazione nel Contesto della Produzione Farmaceutica

16 e 18 aprile 2024

Ricerca Clinica

Normativa della Ricerca Clinica tra Presente e Futuro

Dispositivi Medici / IVD - Dispositivi Medico Diagnostici In Vitro / Medical Affairs / Regolatorio

Advertisement and Promotion Claims for Medical Devices

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

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

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

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

Dal 12 marzo al 18 giugno 2024

GMP Farmaceutico - Good Manufacturing Practices / Soft Skill

Percorso Formativo GMP Project Management

Market Access Farmaceutico

Healthcare Modeling: Interventi per Migliorare Efficacia ed Efficienza delle Cure

Market Access Farmaceutico

Clinical Support Programs: Strategie e Progetti per Favorire le Attività degli HCP