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ENGLISH
ITALIANO
- Archive 2025
NEW
07 May 2025
Pharmacovigilance
Effective Management of SAE/SUSAR Reporting and CIOMS Forms
07 and 09 May 2025
Pharmacovigilance
Pharmacovigilance Agreements
08 maggio 2025
Evidence Generation
/
Medical Affairs
/
Clinical Research
Generare Real World Evidence (RWE) con Metodi Osservazionali
13, 15 e 20 maggio 2025
Medical Affairs
Patient Advocacy ed Engagement in Ambito Farmaceutico ed Healthcare
13 e 15 maggio 2025
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Regulatory
Patient Support Program (PSP) e Compliance: quali Normative Considerare?
14 May 2025
Soft Skill
Great Topic – Shame About the Slides!
NEW
14 and 15 May 2025
GMP (Good Manufacturing Practices)
Biologics and Biosimilars Manufacturing
14 maggio 2025
Evidence Generation
/
Medical Affairs
Progettare e Comunicare in Medical Affairs
15 and 16 May 2025
Medical Device
Labelling Requirements for Medical Devices
15, 20 and 22 May 2025
Pharmacovigilance
/
Regulatory
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
NEW
19 and 21 May 2025
Animal Health
/
Regulatory
Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices
NEW
20 and 22 May 2025
Regulatory
Cosmetics in the EU, US and Canada
20 e 27 maggio 2025
Medical Affairs
Organizzare Hospital Meeting di Successo: Strategie e Competenze Essenziali
NEW
21 maggio 2025
GMP (Good Manufacturing Practices)
ICH Q14: Lo Sviluppo di Metodi Analitici
22 and 23 May 2025
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Person Responsible for Regulatory Compliance (PRRC) – An MDR/IVDR Requirement
22 maggio 2025
Regulatory
Etichettatura degli Integratori Alimentari - Applichiamo la Normativa ad Esempi Reali
22 e 23 maggio 2025
Medical Affairs
/
Soft Skill
La Gestione dell’Advisory Board nei Progetti Life Science
NEW
27 e 29 maggio 2025
Clinical Research
La Valutazione di Impatto della Protezione dei Dati (DPIA) nella Ricerca Clinica
NEW
27 e 28 maggio 2025
GMP (Good Manufacturing Practices)
I Risvolti Pratici del Regolamento (UE) n. 536/2014 sulle Sperimentazioni Cliniche (CTR 536/2014)
28 May 2025
Medical Device
/
Medical Affairs
/
Clinical Research
/
Soft Skill
Oral Presentations
NEW
03, 04 e 10 giugno 2025
GMP (Good Manufacturing Practices)
ICH Q2 (R2): Le Novità nella Convalida dei Metodi Analitici
03, 05 e 10 giugno 2025
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Statistica Medica per Non Statistici
04, 05 and 06 June 2025
Medical Affairs
/
Medical Writing
Writing Articles for Peer-Reviewed Journals: Comprehensive Strategies from the Concept to Successful Publication
04 e 06 giugno 2025
Pharmacovigilance
La Gestione del Case Processing in Farmacovigilanza
05 June 2025
Regulatory
Electronic Submissions and Data Management in Regulatory Affairs
05 and 06 June 2025
Medical Device
/
Regulatory
Clinical Evaluation for Medical Devices
06 June 2025
Pharmacovigilance
German Pharmacovigilance Day
09, 13 e 16 giugno 2025
Regulatory
/
Clinical Research
Computer System Validation (CSV) - GxP Process Owner and Quality Assurance: In or Out?
NEW
11 e 12 giugno 2025
Medical Affairs
Digital Support Services (D-SS): l’Evoluzione Digitale dei Servizi di Supporto al Paziente per una Migliore Assistenza Terapeutica
NEW
11 and 12 June 2025
Medical Device
/
GMP (Good Manufacturing Practices)
/
Regulatory
/
Clinical Research
Good Distribution Practices (GDP) of Medicinal Products and Medical Devices
13 and 20 June 2025
Pharmacovigilance
The PSMF (Pharmacovigilance System Master File): from GVPs to Inspections
17 and 19 June 2025
Pharmacovigilance
Pharmacovigilance System: Audit & Inspection Readiness
19 June 2025
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
NEW
19 e 20 giugno 2025
Medical Device
/
Regulatory
I Combination Products ai Sensi del Regolamento UE sui Dispositivi Medici (MDR)
19, 23 and 25 June 2025
Clinical Research
/
Statistics and Data Management
A Practical Guide to Innovative Trial Design
NEW
23 June 2025
Regulatory
Food Supplement Regulations in the EU
24, 25 and 26 June 2025
Medical Writing
Tips and Tricks to Improve your Technical/Scientific Writing
NEW
26 e 27 giugno 2025
Regulatory
La Pubblicità degli Integratori Alimentari: Applichiamo la Teoria alla Pratica
27 giugno 2025
Clinical Research
Qualifica dei Vendor nella Ricerca Clinica - Approfondimenti
01 July 2025
Medical Device
What You Need to Know about Medical Device Software and Never Dared to Ask
02 July 2025
GMP (Good Manufacturing Practices)
Human Error: the True Root Cause of a Deviation?
07 July 2025
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Writing Science for Lay Audiences
From 17 September to 22 October 2025
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents in the Life Cycle of a Medicinal Product
17 September 2025
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Basic Concepts and Definitions for Pharmacovigilance Writing
17, 18 and 22 September 2025
Medical Device
How to Write a Clinical Evaluation Plan and Report
22 e 23 settembre 2025
Medical Device
/
Regulatory
La Biocompatibilità e la Caratterizzazione Chimica: Dispositivi Medici Sicuri
22 September 2025
Pharmacovigilance
The “Global” Qualified Person Responsible for Pharmacovigilance (QPPV) Workshop
22 e 23 settembre 2025
GMP (Good Manufacturing Practices)
EU GMP Annex 15 - La Qualifica e la Convalida nell'Industria Farmaceutica
NEW
23, 25 and 30 September 2025
Pharmacovigilance
Signal Detection and Signal Management
24 e 26 settembre 2025
Pharmacovigilance
/
GMP (Good Manufacturing Practices)
/
Clinical Research
Buone Pratiche per la Gestione dei Documenti Cartacei e dei Dati Elettronici in Ambito GxP
24 e 25 settembre 2025
Medical Device
ISO 14155/2020 - Come Svolgere uno Studio Clinico con Dispositivi Medici
24 September 2025
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on Signal Management and Development Safety Update Reports (DSUR)
25 and 29 September 2025
Medical Writing
/
Clinical Research
Writing Clinical Study Reports
dal 26 settembre al 22 novembre 2025
Clinical Research
Clinical Quality Assurance: un Ruolo Chiave nella Ricerca Clinica
NEW
29 September 2025
Animal Health
/
Pharmacovigilance
Veterinary QPPV Oversight
30 settembre e 02 ottobre 2025
Regulatory
Cosmetici - Aspetti Tecnico-Regolatori e Panorama Normativo
30 settembre e 01 ottobre 2025
Soft Skill
Comunicare con l'Intelligenza Relazionale
01 ottobre 2025
Pharmacovigilance
Italian Pharmacovigilance Day
01 October 2025
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on the Risk Management Plan (RMP)
NEW
01 e 03 ottobre 2025
Market Access
Market Access: Conoscere e Anticipare le Sfide del Settore Sanità per Garantire un Accesso Omogeneo e Sostenibile ai Farmaci
NEW
02, 07 e 09 ottobre 2025
GMP (Good Manufacturing Practices)
Packaging Primario per Farmaci Parenterali: Combinare aspetti regolatori e tecnici per una somministrazione sicura ed efficace
07, 09, 14 e 16 ottobre 2025
Clinical Research
Selezione e Convalida di Una Soluzione Cloud in Ambito GxP
NEW
07 ottobre 2025
Medical Affairs
/
Clinical Research
Il Futuro della Raccolta Dati nella Ricerca Clinica: Digital Endpoints e Digital Evidence
NEW
08 October 2025
Animal Health
/
Pharmacovigilance
Veterinary Pharmacovigilance System
08 October and 13 October 2025
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on the Periodic Safety Update Report (PSUR)
08 and 09 October 2025
Medical Device
/
Medical Writing
State of the Art Section for Medical Devices – Unpacking the Tips and Tricks of a Complex Document
09 and 10 October 2025
Medical Device
/
Regulatory
Combination Products under the EU Medical Devices Regulation (MDR)
NEW
13 and 14 October 2025
GMP (Good Manufacturing Practices)
Mastering Continuous Process Validation in Pharmaceutical Manufacturing
13 and 14 October 2025
Medical Device
MedDev Day
14, 21 October 2025 | 11, 18 November 2025
Evidence Generation
/
Medical Affairs
/
Clinical Research
A Systematic Approach to Real World Evidence (RWE) Generation in Life Sciences - a 2 step intensive course
14 e 21 ottobre 2025
Medical Affairs
/
Regulatory
/
Clinical Research
Off-Label, Uso Compassionevole e Accesso Precoce (Early Access)
NEW
15 e 16 ottobre 2025
Medical Affairs
/
Medical Writing
Strumenti di Intelligenza Artificiale e Conformità all’AI Act per Professionisti del Medical Affair: Esercizi ed Esempi Pratici
NEW
15 e 22 ottobre 2025
Medical Affairs
/
Clinical Research
Terapie Digitali (DTx): a che Punto Siamo?
15 and 16 October 2025
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
16 October 2025
Medical Affairs
/
Medical Writing
/
Soft Skill
How to Create Effective Visuals for Better Communicating your Science
NEW
16 e 17 ottobre 2025
GMP (Good Manufacturing Practices)
Gestione Efficace delle Deviazioni in Ambito GMP
17 ottobre 2025
Medical Affairs
/
Regulatory
/
Clinical Research
I Radiofarmaci
NEW
20, 23 e 27 ottobre 2025
GMP (Good Manufacturing Practices)
Technology Transfer Farmaceutico
NEW
20 October 2025
Regulatory
Cosmetovigilance in the EU
21 and 22 October 2025
Medical Device
Initiating the Development of Artificial Intelligence (AI) Medical Devices
22, 23 and 24 October 2025
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Clinical Study Protocols – Structure & Content
22 October 2025
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on Addendum to the Clinical Overview (AddCO) and Referrals
NEW
23 ottobre 2025
Medical Affairs
Dal Riconoscimento alla Raccolta degli Insights
27 and 28 October 2025
Statistics and Data Management
European Statistical Forum
NEW
28 October 2025
Animal Health
/
Pharmacovigilance
Veterinary Signal Detection
28 and 29 October 2025
GMP (Good Manufacturing Practices)
Ensuring Excellence in (Bio)pharmaceutical Cleaning Validation
28, 31 ottobre e 04 novembre 2025
Medical Device
/
Market Access
Il Market Access per i Dispositivi Medici
29 and 30 October 2025
Medical Device
/
Medical Affairs
/
Clinical Research
Medical Reading
03, 05, 10 e 12 novembre 2025
Pharmacovigilance
/
Clinical Research
Safety Management e Farmacovigilanza
NEW
03, 04 and 05 November 2025
Medical Device
/
GMP (Good Manufacturing Practices)
/
Regulatory
Ethylene Oxide Sterilization for Medical Devices: Principles, Validation, and Regulatory Compliance
04, 06 e 11 novembre 2025
Regulatory
Integratori Alimentari - Aspetti Tecnico-Regolatori e Panorama Normativo
05 and 07 November 2025
Pharmacovigilance
/
Medical Affairs
/
Clinical Research
Beyond PubMed
10, 14 e 17 novembre 2025
Clinical Research
Audit to Computer Systems
NEW
10 and 11 November 2025
Medical Device
/
Regulatory
Pre-Market Submission of Medical Devices to the US FDA: Navigating the Pre-Sub and 510(k) Process
11 e 13 novembre 2025
Medical Device
/
Regulatory
La Vigilanza Post Market per i Dispositivi Medici secondo MDR e FDA
11 November 2025
Pharmacovigilance
Nordic Pharmacovigilance Day
12 e 19 novembre 2025
Regulatory
Terapie Geniche e Terapie Cellulari
13 and 18 November 2025
GMP (Good Manufacturing Practices)
/
Regulatory
Advanced Therapy Medicinal Product (ATMP): a Roadmap from Classification to Regulation and Manufacturing
NEW
13 November 2025
Animal Health
/
Pharmacovigilance
Veterinary Pharmacovigilance Quality Management
NEW
17 and 18 November 2025
Medical Affairs
/
Medical Writing
Hands-On Lab on AI Tools and Compliance with AI Act for Medical Affairs Professionals
20 and 25 November 2025
Evidence Generation
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Protocol Writing and Communication of Real World Evidence
26 and 27 November 2025
Animal Health
/
Pharmacovigilance
Introduction to Veterinary Pharmacovigilance
26 November 2025
Regulatory
Decoding Electronic Product Information (ePI)
Data TBD
Medical Affairs
/
Regulatory
Codice Deontologico di Farmindustria e le Linee Guida per la Certificazione delle Attività di Informazione Scientifica: come applicarle in Azienda
Data TBD
Regulatory
La Pubblicità del Farmaco
07 e 09 maggio 2025
IVDs (In-Vitro Diagnostics)
La Sorveglianza Post-Market dei Dispositivi Diagnostici in Vitro
08, 10, 15 e 17 aprile 2025
Pharmacovigilance
Il Sistema di Qualità Applicato alla Farmacovigilanza
17 April 2025
GMP (Good Manufacturing Practices)
Introduction to Aseptic Process Simulation (APS)
15 e 16 aprile 2025
Clinical Research
Protezione dei dati personali (GDPR) e Ricerca Scientifica
16 April 2025
Medical Device
From Good to Excellent: The Summary of Safety and Clinical Performance (SSCP)
Dal 21 febbraio al 16 aprile 2025
Medical Affairs
Medical Affairs Essentials
15 aprile 2025
Medical Affairs
Progettare un Patient Support Program (PSP): Configurazione del Processo e Strumenti
11 aprile 2025
Clinical Research
ICH GCP (R3)
11 April 2025
Clinical Research
Master the New Swiss Clinical Trial Framework and its Interplay with the EU CTR - Similarities and Differences
08 e 10 aprile 2025
Medical Affairs
Il Responsabile del Servizio Scientifico
10 April 2025
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
08 e 10 aprile 2025
Regulatory
/
Clinical Research
Normativa della Ricerca Clinica tra Presente e Futuro
08 April 2025
Medical Device
Select the Ideal PMCF Strategy for a Medical Device
31 March and 03 April 2025
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Searching the Medical Literature
14 and 15 April 2025
Regulatory
Mastering the Essentials of Marketing Authorisation Application (MAA): A Path to Regulatory Success in the EU, UK and US
27 and 28 March 2025
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
26 March 2025
Pharmacovigilance
Attributability and Causality in Pharmacovigilance: Still a Hot Topic
25 e 26 marzo 2025
GMP (Good Manufacturing Practices)
Annex 1 e Contamination Control Strategy
20 e 21 marzo 2025
Medical Affairs
/
Clinical Research
/
Soft Skill
Dalla Comunicazione Professionale alla Negoziazione
11, 18 e 20 marzo 2025
GMP (Good Manufacturing Practices)
La Qualifica dei Fornitori GMP
19 marzo 2025
Medical Affairs
/
Clinical Research
Il Consenso quale Base Giuridica per il Trattamento Dati nella Ricerca Clinico-Scientifica
01 and 02 April 2025
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
12 e 14 marzo 2025
Medical Device
/
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Ricerca della Letteratura Scientifica: dal Quesito ai Risultati
12 and 13 March 2025
Medical Device
/
Medical Writing
Mastering MDCG 2024-3: Comprehensive Training on Clinical Investigation Plans
25 and 26 March 2025
Clinical Research
How to Implement the EU CTR in Sponsor Organisations to Ensure Compliance: A Practical Approach
20 and 24 February 2025
Animal Health
/
Pharmacovigilance
Reporting Requirements in Veterinary Pharmacovigilance
20 and 21 February 2025
Medical Device
Labelling Requirements for Medical Devices
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