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ENGLISH
ITALIANO
- Archive 2023
21, 23, 28 e 30 novembre 2023
Pharmacovigilance
/
Clinical Research
Safety Management e Farmacovigilanza
28 November 2023
Medical Device
From Good to Excellence: State of the Art Section for Medical Devices Inside-Out
24 November 2023
Pharmacovigilance
Veterinary Pharmacovigilance: Suspected Adverse Event and Signal Management
dal 29 settembre al 25 novembre 2023
Clinical Research
Clinical Quality Assurance: un Ruolo Chiave nella Ricerca Clinica
21 e 23 novembre 2023
Regulatory
Integratori Alimentari - Aspetti Tecnico-Regolatori e Panorama Normativo
21 e 22 novembre 2023
Medical Device
/
Regulatory
Dispositivi Medici Sicuri – La Biocompatibilità e la Caratterizzazione Chimica
22 November 2023
Medical Writing
/
Soft Skill
How to Create Effect Visuals for Better Communicating your Science
08, 15 and 22 November 2023
Medical Affairs
/
Clinical Research
/
Statistics and Data Management
All You Need to Know to Understand Statistic if You are not a Statistician
04 e 05 dicembre 2023
Medical Device
/
Regulatory
Il Processo di Gestione dei Rischi applicato ai Dispositivi Medici
16 November 2023
Pharmacovigilance
Nordic Pharmacovigilance Day
14 e 16 novembre 2023
Medical Device
/
Regulatory
La Vigilanza Post Market per i Dispositivi Medici secondo MDR e FDA
15 and 16 November 2023
Medical Device
Initiating the Development of Artificial Intelligence (AI) Medical Devices
13 e 14 novembre 2023
Clinical Research
Condurre uno Studio Clinico Adempiendo alla Normativa GDPR: un Ponte fra Good Clinical Practices (GCP) e General Data Protection Regulation (GDPR)
14 November 2023
Statistics and Data Management
European Statistical Forum
13 novembre 2023
Regulatory
Navigare le Novità: le Ultime Revisioni al Codice Deontologico di Farmindustria e le Linee Guida per la Certificazione delle Attività Scientifiche
09 e 10 novembre 2023
Pharmacovigilance
La Gestione del Case Processing in Farmacovigilanza
09 November 2023
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Medical Affairs
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
06 and 08 November 2023
Evidence Generation
/
Market Access
/
Medical Affairs
/
Clinical Research
Patient Registries as a Source of Real-World Evidence not only for Pharmaceuticals but also for Medical Devices
22, 24 and 27 November 2023
Medical Affairs
Patient Advocacy and Engagement in Pharmaceutical Companies
20 e 23 novembre 2023
Market Access
Il Market Access a Supporto del Time to Market
25 e 27 ottobre 2023
Regulatory
Off-Label, Uso Compassionevole ed Expanded Access Program. Come Orientarsi tra Normative, Studi, Ricerca e Realtà Clinica
25 and 26 October 2023
Medical Writing
/
Clinical Research
Clinical Study Reports – a 360° Perspective
25 and 26 October 2023
Medical Device
What You Need to Know about Medical Device Software and Never Dared to Ask
24 and 26 October 2023
GMP (Good Manufacturing Practices)
/
Regulatory
Advanced Therapy Medicinal Product (ATMP) Roadmap from Classification to Regulation and Manufacturing
26 ottobre 2023
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Ricerca della Letteratura Scientifica: come Sfruttare le Risorse Gratuite in Rete
17, 19 and 24 October 2023
Medical Device
/
Evidence Generation
/
Medical Affairs
/
Clinical Research
Generating Real World Evidence (RWE) with Observational Methods
24 October 2023
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Writing Science for Lay Audiences
16 e 21 novembre 2023
Regulatory
Technology Transfer e Proprietà Intellettuale
07, 09 and 14 November 2023
Pharmacovigilance
Benefit Risk Assessment in Pharmacovigilance
07 e 08 novembre 2023
Medical Device
Medical Device Software
07 November 2023
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
How to Become a Successfully Published Author - Practical steps to make the publication process as smooth and as successful as possible
03, 10, 17 e 20 ottobre 2023
Pharmacovigilance
Qualità in Farmacovigilanza
19 ottobre 2023
Pharmacovigilance
Italian Pharmacovigilance Day
17 and 19 October 2023
Regulatory
The Basics of Regulatory Affairs for Cosmetic Products in US and Canada
17 and 19 October 2023
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
From 13 September to 18 October 2023
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents in the Life Cycle of a Medicinal Product
13 November 2023
Clinical Research
/
Statistics and Data Management
Design and Analysis of Clinical Trials in the Era of Precision Medicine
18 October 2023
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on Addendum to the Clinical Overview (AddCO) and Referrals
11 e 13 ottobre 2023
Regulatory
Cosmetici - Aspetti Tecnico-Regolatori e Panorama Normativo
10 and 11 October 2023
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
10 ottobre 2023
Medical Affairs
/
Regulatory
/
Clinical Research
Terapie Geniche e Terapie Cellulari
28 September and 11 October 2023
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on the Periodic Safety Update Report (PSUR)
23 and 25 October 2023
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Beyond PubMed
04, 05 and 06 October 2023
Medical Affairs
/
Medical Writing
Clinical Study Protocols – Structure & Content
05 October 2023
Regulatory
Electronic Submissions and Data Management in Regulatory Affairs
05 e 06 October 2023
Medical Device
/
Regulatory
Fundamentals of Medical Device US FDA Pre-Market Submissions
20 e 27 ottobre 2023
GMP (Good Manufacturing Practices)
Audit GMP: la Qualifica della Supply Chain
02 e 04 ottobre 2023
Regulatory
Gestione della Proprietà Industriale - Il Brevetto a Tutela delle Invenzioni
19 and 20 October 2023
Soft Skill
What you Need to Know about Management and never Dared to Ask
27 e 29 settembre 2023
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Ricerca della Letteratura Scientifica: dal Quesito ai Risultati
27 e 29 settembre 2023
Pharmacovigilance
/
GMP (Good Manufacturing Practices)
/
Clinical Research
Buone Pratiche per la Gestione dei Documenti Cartacei e dei Dati Elettronici in Ambito GxP
25 and 26 September 2023
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Searching the Medical Literature
26 September 2023
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on the Risk Management Plan (RMP)
12 e 13 ottobre 2023
Medical Device
/
Regulatory
L’Ingegneria dell’Usabilità applicata ai Dispositivi Medici
26 September 2023
Medical Device
MedDev Day
11, 18 e 25 ottobre 2023
Medical Device
/
Market Access
Il Market Access per i Dispositivi Medici
25 September 2023
Medical Device
From Good to Excellent: The Summary of Safety and Clinical Performance (SSCP)
19, 20 and 21 September 2023
Medical Writing
Tips and Tricks to Improve your Technical/Scientific Writing
19 e 21 settembre 2023
Medical Device
/
Regulatory
/
Clinical Research
ISO 14155/2020 - Come Svolgere uno Studio Clinico con Dispositivi Medici
20 September 2023
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on Signal Management and Development Safety Update Reports (DSUR)
20 September 2023
Pharmacovigilance
German Pharmacovigilance Day
12, 14 e 19 settembre 2023
Pharmacovigilance
Signal Detection e Signal Management
04 ottobre 2023
Medical Device
/
Evidence Generation
/
Medical Affairs
Come Produrre Dati Non Clinici e Comunicare Contenuti Scientifici in Poco Tempo? Elementare, Watson!
26, 27 e 28 settembre 2023
Soft Skill
Comunicare con l'Intelligenza Relazionale - La Flessibilità nelle Relazioni per Comunicare, Guidare e Motivare Colleghi e Interlocutori, in Presenza e da Remoto
13 September 2023
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Basic Concepts and Definitions for Pharmacovigilance Writing
13 settembre 2023
Regulatory
Integratori Alimentari a Base di Botanicals
03 e 05 ottobre 2023
Evidence Generation
Corso avanzato per la Progettazione di uno Studio Osservazionale Pre o Post Marketing
26 and 28 September 2023
Evidence Generation
/
Market Access
/
Medical Affairs
/
Clinical Research
How Are You? – Asking the Patients - Patient-Reported Outcomes (PRO) with Focus on Measuring Quality of Life (QoL)
18 e 20 settembre 2023
Medical Device
/
Regulatory
La Valutazione Clinica di un Dispositivo Medico
19 settembre 2023
GMP (Good Manufacturing Practices)
/
Soft Skill
Lean Six Sigma nel Mondo Farmaceutico - Strumenti “LEAN” per l’Ottimizzazione dei Processi in Ambito Good Manufacturing Practices (GMP)
05 luglio 2023
Regulatory
Integratori Alimentari ed Advertising - Caratteristiche di una Corretta Comunicazione Commerciale e Vincoli Normativi
28 and 30 June 2023
Pharmacovigilance
Pharmacovigilance System: Audit & Inspection Readiness
07, 14, 21 e 28 giugno 2023
Pharmacovigilance
Qualità in Farmacovigilanza
22, 23 and 27 June 2023
Pharmacovigilance
/
Regulatory
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
20 and 22 June 2023
Regulatory
Fundamentals of European Cosmetics Regulatory Affairs
21 and 22 June 2023
Medical Device
/
Regulatory
Combination Products under the EU Medical Devices Regulation (MDR)
21 giugno 2023
Medical Affairs
/
Regulatory
/
Clinical Research
I Trasferimenti dei Dati Personali extra SEE
13, 15 e 20 giugno 2023
Medical Affairs
Patient Support Program (PSP) - Dalla Strategia al Management
12 e 19 giugno 2023
Medical Affairs
Hospital Meeting: come Pianificare e Condurre una Riunione di Successo
Dal 01 marzo al 19 giugno 2023
GMP (Good Manufacturing Practices)
/
Soft Skill
Percorso Formativo GMP Project Management
28 June 2023
Soft Skill
Great Topic – Shame About the Slides!
04, 06 e 11 luglio 2023
Market Access
Regolamento Europeo di Health Technology Assessment (EU-HTA)
20, 23 e 27 giugno 2023
Clinical Research
/
Soft Skill
La Ricerca Clinica e l’Efficacia della Comunicazione nel Lavoro di Gruppo
16 giugno 2023
GMP (Good Manufacturing Practices)
ICH Q9 Quality Risk Management
14 and 15 June 2023
Medical Device
/
Regulatory
The EU Regulation 2017/745 on Medical Devices
14 giugno 2023
GMP (Good Manufacturing Practices)
/
Regulatory
/
Clinical Research
GAMP 5 A Risk-Based Approach to Compliant GxP Computerized Systems- Release 2
12 and 13 June 2023
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
16, 18, 23 maggio e 01 giugno 2023
Clinical Research
Selezione e Convalida di Una Soluzione Cloud in Ambito GxP
24, 26 and 31 May 2023
Pharmacovigilance
The Pharmacovigilance System Master File (PSMF): from GVPs to Inspections
30 May 2023
Soft Skill
Oral Presentations
12 and 14 June 2023
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
12, 13, 19 e 20 giugno 2023
Soft Skill
Selling with Papers: la Comunicazione dei Risultati Clinici
24 and 26 May 2023
Medical Device
/
Medical Affairs
/
Clinical Research
Medical Reading
25 e 26 maggio 2023
Medical Affairs
/
Soft Skill
La Gestione dell’Advisory Board nei Progetti Life Science
09, 12 e 16 giugno 2023
Regulatory
/
Clinical Research
Computer System Validation - GxP Process Owner and Quality Assurance: In or Out?
16, 18 e 23 maggio 2023
Evidence Generation
Generare Real World Evidence (RWE) con Metodi Osservazionali
23 maggio 2023
Clinical Research
Qualifica dei Vendor nella Ricerca Clinica - Approfondimenti
17, 19 e 22 maggio 2023
Medical Affairs
Patient Advocacy ed Engagement nell’Azienda Farmaceutica
18 and 19 May 2023
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
New MDR/IVDR Requirement: the ‘Person Responsible for Regulatory Compliance’ (PRRC)
17 e 18 maggio 2023
IVDs (In-Vitro Diagnostics)
La Sorveglianza Post-Market dei Dispositivi Diagnostici in Vitro
04, 11 and 12 May 2023
Pharmacovigilance
/
Regulatory
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
09 e 11 maggio 2023
Regulatory
La Pubblicità del Farmaco
From 28 February to 05 May 2023
Medical Device
Medical Devices: a 4-Step Clinical Evaluation Masterclass
05 May 2023
Medical Device
The Summary of Safety and Clinical Performance (SSCP)
03 e 04 maggio 2023
Medical Device
/
Regulatory
La Registrazione dei Dispositivi Medici presso FDA
26 and 28 April 2023
Medical Device
Knowing your Post-Market Clinical Follow-up (PMCF)
18 e 20 aprile 2023
Clinical Research
Normativa della Ricerca Clinica tra Presente e Futuro
18 e 19 aprile 2023
IVDs (In-Vitro Diagnostics)
/
Clinical Research
La Conduzione di uno Studio Clinico con un Dispositivo Medico-Diagnostico in Vitro
12 April 2023
Pharmacovigilance
Pharmacovigilance Agreements
04 e 06 aprile 2023
Medical Affairs
Il Responsabile del Servizio Scientifico
06 April 2023
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Medical Affairs
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
20 and 21 April 2023
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
How to Globally Register a Medical Device
21, 23 e 28 marzo 2023
Medical Affairs
/
Clinical Research
/
Statistics and Data Management
La Statistica Medica per Non Statistici
28 marzo 2023
Medical Affairs
/
Regulatory
/
Clinical Research
Il Consenso quale Base Giuridica per il Trattamento Dati nella Ricerca Clinico-Scientifica
27 marzo 2023
Medical Affairs
/
Regulatory
/
Clinical Research
I Radiofarmaci
22 and 23 March 2023
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
22 March 2023
Pharmacovigilance
“Attributability” in Pharmacovigilance: Still a Hot Topic
14, 16 and 21 March 2023
Medical Device
How to Write a Clinical Evaluation Plan and Report
09 e 20 marzo 2023
GMP (Good Manufacturing Practices)
Annex 1 e la Contamination Control Strategy
28, 29, 31 marzo 2023
Medical Affairs
/
Medical Writing
/
Regulatory
Struttura e Contenuti del Protocollo di uno Studio Clinico
30 marzo e 04 aprile 2023
Evidence Generation
/
Market Access
/
Medical Affairs
Utilizzo dei Dati Derivanti dai PSP: Confini e Opportunità
28 febbraio e 02 marzo 2023
Clinical Research
General Data Protection Regulation (GDPR), Ricerca Scientifica e Norme Locali
01 and 02 March 2023
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
28 February and 01 March 2023
Medical Device
/
Regulatory
Clinical Evaluation for Medical Devices
01 March 2023
Regulatory
/
Clinical Research
Clinical Trials Information System (CTIS) Interactive Demo
18 ottobre 2023
Evidence Generation
/
Clinical Research
La Privacy nella Ricerca Osservazionale
