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ENGLISH
ITALIANO
- Archive 2024
14, 19 e 21 marzo 2024
Medical Affairs
/
Clinical Research
/
Statistics and Data Management
La Statistica Medica per Non Statistici
20 March 2024
Pharmacovigilance
“Attributability” in Pharmacovigilance: Still a Hot Topic
20, 21 and 25 March 2024
Medical Device
How to Write a Clinical Evaluation Plan and Report
26 e 27 marzo 2024
GMP (Good Manufacturing Practices)
Annex 1 e Contamination Control Strategy
26 marzo 2024
Medical Affairs
/
Regulatory
/
Clinical Research
Il Consenso quale Base Giuridica per il Trattamento Dati nella Ricerca Clinico-Scientifica
03, 04 and 05 April 2024
Medical Affairs
/
Medical Writing
Clinical Study Protocols – Structure & Content
NEW
03 e 05 aprile 2024
GMP (Good Manufacturing Practices)
Le Sfide della Produzione di un Investigational Medicinal Product (IMP)
09 e 10 aprile 2024
IVDs (In-Vitro Diagnostics)
/
Clinical Research
La Conduzione di uno Studio Clinico con un Dispositivo Medico-Diagnostico in Vitro
09 e 11 aprile 2024
Medical Affairs
Il Responsabile del Servizio Scientifico
10, 17 e 24 aprile 2024
Medical Device
/
Market Access
Il Market Access per i Dispositivi Medici
10 aprile 2024
Medical Affairs
/
Regulatory
/
Clinical Research
I Radiofarmaci
10 and 11 April 2024
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
15 and 18 April 2024
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Searching the Medical Literature
16 e 18 aprile 2024
Clinical Research
Normativa della Ricerca Clinica tra Presente e Futuro
17 aprile 2024
Regulatory
Integratori Alimentari ed Advertising
18 April 2024
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Medical Affairs
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
NEW
22 aprile 2024
GMP (Good Manufacturing Practices)
La Compliance ai Requisiti GMP: Ruolo e Funzioni dell’Assicurazione Qualità
NEW
23 aprile 2024
Medical Affairs
Progettare un Patient Support Program (PSP): Configurazione del Processo e Strumenti
NEW
23 April 2024
Medical Device
Select the Ideal PMCF Strategy for a Medical Device
29 April 2024
Medical Device
From Good to Excellent: The Summary of Safety and Clinical Performance (SSCP)
NEW
07 e 14 maggio 2024
GMP (Good Manufacturing Practices)
Audit ai Fornitori come Strumento per la Qualifica della Supply Chain Farmaceutica
07 e 09 maggio 2024
Regulatory
La Pubblicità del Farmaco
NEW
08, 15, 22 May and 10, 17 October 2024
Evidence Generation
/
Medical Affairs
/
Clinical Research
A Systematic Approach to Real World Evidence (RWE) Generation in Life Sciences - A 2 Step Intensive Course
08 maggio 2024
Medical Affairs
Progettare e Comunicare in Medical Affairs
NEW
09 e 10 maggio 2024
GMP (Good Manufacturing Practices)
Agile Project Management: Gestire l’Innovazione nel Contesto della Produzione Farmaceutica
13, 15 and 16 May 2024
Medical Device
How to Write a Clinical Evaluation Plan and Report
14, 16 e 21 maggio 2024
Medical Affairs
Patient Advocacy ed Engagement nell’Azienda Farmaceutica
15 e 16 maggio 2024
IVDs (In-Vitro Diagnostics)
La Sorveglianza Post-Market dei Dispositivi Diagnostici in Vitro
16 and 17 May 2024
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Person Responsible for Regulatory Compliance (PRRC) - An MDR/IVDR Requirement
21 and 22 May 2024
Pharmacovigilance
Pharmacovigilance Agreements
21, 24 and 28 May 2024
Pharmacovigilance
/
Regulatory
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
NEW
22 maggio 2024
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Regulatory
Patient Support Program (PSP) e Compliance: quali Normative Considerare?
NEW
22 maggio 2024
Regulatory
Etichettatura degli Integratori Alimentari - Applichiamo la Normativa ad Esempi Reali
22 May 2024
Soft Skill
Beyond Slide Decks
NEW
23 and 29 May 2024
Pharmacovigilance
Introduction to Veterinary Pharmacovigilance
NEW
23 and 27 May 2024
Regulatory
Marketing Authorization Application in EU, US and UK
23 e 24 maggio 2024
Medical Affairs
/
Soft Skill
La Gestione dell’Advisory Board nei Progetti Life Science
27 May 2024
Soft Skill
Oral Presentations
28 e 30 maggio 2024
Medical Affairs
Il Responsabile del Servizio Scientifico
28 and 29 May 2024
Medical Device
/
Medical Affairs
/
Clinical Research
Medical Reading
NEW
29 May 2024
Regulatory
Decoding Electronic Product Information (ePI)
04, 06 e 11 giugno 2024
Pharmacovigilance
Signal Detection e Signal Management
04 e 06 giugno 2024
Clinical Research
General Data Protection Regulation (GDPR), Ricerca Scientifica e Norme Locali
04 June 2024
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
05 e 06 giugno 2024
Soft Skill
Comunicare con l'Intelligenza Relazionale
05 e 07 giugno 2024
Pharmacovigilance
La Gestione del Case Processing in Farmacovigilanza
NEW
05, 07, 12 e 14 giugno 2024
Pharmacovigilance
Il Sistema di Qualità Applicato alla Farmacovigilanza
05 giugno 2024
GMP (Good Manufacturing Practices)
ICH Q9 Quality Risk Management
10, 14 e 17 giugno 2024
Regulatory
/
Clinical Research
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
NEW
11 e 12 giugno 2024
GMP (Good Manufacturing Practices)
Le Good Calibration Practices (GCalP) negli Impianti Automatici di Produzione
NEW
12 e 13 giugno 2024
Medical Affairs
Il Patient Support Program (PSP) e la Transizione Digitale: Opportunità e Rischi
NEW
13 June 2024
GMP (Good Manufacturing Practices)
Human Error: the True Root Cause of a Deviation?
14 and 21 June 2024
Pharmacovigilance
The PSMF (Pharmacovigilance System Master File): from GVPs to Inspections
NEW
18, 24 and 27 June 2024
Clinical Research
/
Statistics and Data Management
A Practical Guide to Innovative Trial Design
18 and 20 June 2024
Pharmacovigilance
Pharmacovigilance System: Audit & Inspection Readiness
18 and 20 June 2024
Regulatory
Fundamentals of European Cosmetics Regulatory Affairs
19 and 20 June 2024
Medical Device
/
Regulatory
Combination Products under the EU Medical Devices Regulation (MDR)
NEW
24 and 26 June 2024
GMP (Good Manufacturing Practices)
Biologics and Biosimilars Manufacturing
NEW
25 and 26 June 2024
Pharmacovigilance
Reporting Requirements in Veterinary Pharmacovigilance
25 e 27 giugno, 2 e 4 luglio 2024
Clinical Research
Selezione e Convalida di Una Soluzione Cloud in Ambito GxP
NEW
26 and 27 June 2024
Medical Device
/
Regulatory
/
Clinical Research
Good Distribution Practices of Medical Devices
NEW
26 giugno 2024
Regulatory
Integratori Alimentari e Advertising: Applichiamo la Teoria alla Pratica
28 giugno 2024
Clinical Research
Qualifica dei Vendor nella Ricerca Clinica - Approfondimenti
NEW
02 July 2024
GMP (Good Manufacturing Practices)
Statistical Process Control for Pharmaceutical Manufacturing
NEW
16 September 2024
GMP (Good Manufacturing Practices)
Quality by Design
NEW
17 and 18 September 2024
Pharmacovigilance
Introduction to Pharmacovigilance
17 September 2024
Pharmacovigilance
German Pharmacovigilance Day
17, 18 and 19 September 2024
Medical Writing
Tips and Tricks to Improve your Technical/Scientific Writing
From 18 September to 23 October 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents in the Life Cycle of a Medicinal Product
18 September 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Basic Concepts and Definitions for Pharmacovigilance Writing
NEW
18 e 19 settembre 2024
GMP (Good Manufacturing Practices)
EU GMP Annex 15 - La Qualifica e la Convalida nell'industria farmaceutica
23 e 24 settembre 2024
Medical Device
/
Regulatory
La Biocompatibilità e la Caratterizzazione Chimica: Dispositivi Medici Sicuri
NEW
24, 26 settembre e 01 ottobre 2024
Market Access
/
Medical Affairs
/
Regulatory
Patient Support Program (PSP) e Patient Solution: Compiere una Scelta Strategica a Supporto del Paziente
25 e 27 settembre 2024
Pharmacovigilance
/
GMP (Good Manufacturing Practices)
/
Clinical Research
Buone Pratiche per la Gestione dei Documenti Cartacei e dei Dati Elettronici in Ambito GxP
25 September 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on Signal Management and Development Safety Update Reports (DSUR)
25 e 26 settembre 2024
Medical Device
ISO 14155/2020 - Come Svolgere uno Studio Clinico con Dispositivi Medici
dal 27 settembre al 23 novembre 2024
Clinical Research
Clinical Quality Assurance: un Ruolo Chiave nella Ricerca Clinica
NEW
27 settembre 2024
Regulatory
Codice Deontologico di Farmindustria e le Linee Guida per la Certificazione delle Attività Scientifiche: come applicarle in azienda
NEW
01 and 02 October 2024
GMP (Good Manufacturing Practices)
Process Validation
01 e 03 ottobre 2024
Regulatory
Cosmetici - Aspetti Tecnico-Regolatori e Panorama Normativo
NEW
01 and 02 October 2024
Medical Device
State of the Art Section for Medical Devices – Unpacking the Tips and Tricks of a Complex Document
2 October 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on the Risk Management Plan (RMP)
Dal 04 ottobre al 13 dicembre 2024
Medical Affairs
Medical Affairs: Prepararsi alle Sfide Future di un Ruolo Complesso
07 and 08 October 2024
Medical Device
MedDev Day
08 e 10 ottobre 2024
Regulatory
Gestione della Proprietà Industriale - Il Brevetto per Tutelare le Invenzioni
09 October and 16 October 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on the Periodic Safety Update Report (PSUR)
09 and 10 October 2024
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
NEW
15 October 2024
GMP (Good Manufacturing Practices)
Introduction to Aseptic Process Simulation (APS)
15 and 17 October 2024
Regulatory
The Basics of Regulatory Affairs for Cosmetic Products in US and Canada
15 and 16 October 2024
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
16 e 23 ottobre 2024
Medical Affairs
/
Regulatory
/
Clinical Research
Off label, Uso Compassionevole e Accesso precoce (Early Access)
17 October 2024
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Soft Skill
How to Create Effective Visuals for Better Communicating your Science
NEW
22 and 23 October 2024
Pharmacovigilance
Veterinary Pharmacovigilance System
22 October 2024
Medical Device
What You Need to Know about Medical Device Software and Never Dared to Ask
23 October 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on Addendum to the Clinical Overview (AddCO) and Referrals
23 and 24 October 2024
Medical Writing
/
Clinical Research
Clinical Study Reports – a 360° Perspective
23 Ottobre 2024
Pharmacovigilance
Italian Pharmacovigilance Day
NEW
28 and 29 October 2024
Medical Device
Initiating the Development of Artificial Intelligence (AI) Medical Devices
NEW
29 and 31 October 2024
GMP (Good Manufacturing Practices)
Cleaning Validation
29 October 2024
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Writing Science for Lay Audiences
30 October and 6 November 2024
GMP (Good Manufacturing Practices)
/
Regulatory
Advanced Therapy Medicinal Product (ATMP) Roadmap from Classification to Regulation and Manufacturing
05, 07, 12 e 14 novembre 2024
Pharmacovigilance
/
Clinical Research
Safety Management e Farmacovigilanza
05 and 07 November 2024
Pharmacovigilance
/
Medical Affairs
/
Clinical Research
Beyond PubMed
06, 13 and 20 November 2024
Medical Affairs
/
Medical Writing
/
Clinical Research
All You Need to Know to Understand Statistic if You are not a Statistician
06, 08 e 13 novembre 2024
Regulatory
Integratori Alimentari - Aspetti Tecnico-Regolatori e Panorama Normativo
NEW
12 and 14 November 2024
GMP (Good Manufacturing Practices)
Sterilization validation
12 e 14 novembre 2024
Medical Device
/
Regulatory
La Vigilanza Post Market per i Dispositivi Medici secondo MDR e FDA
13 e 15 novembre 2024
Clinical Research
Condurre uno Studio Clinico Adempiendo alla Normativa GDPR: un Ponte fra Good Clinical Practices (GCP) e General Data Protection Regulation (GDPR)
13 November 2024
Pharmacovigilance
Nordic Pharmacovigilance Day
NEW
19, 21, 26 and 28 November 2024
GMP (Good Manufacturing Practices)
Computer System Validation (CSV) and Assurance (CSA)
19 and 21 November 2024
Pharmacovigilance
Mastering Benefit Risk Assessment in Pharmacovigilance
NEW
20 and 25 November
Evidence Generation
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Protocol Writing and Communication of Real World Evidence
NEW
03 December 2024
Pharmacovigilance
Veterinary Quality Management
13 and 15 March 2024
Medical Affairs
The Next Generation of Medical Affairs: ChatGPT and Large Language Models (LLMs)
12 and 13 March 2024
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
06 and 07 March 2024
Medical Device
/
Regulatory
Clinical Evaluation for Medical Devices
29 February and 01 March 2024
Medical Device
/
Regulatory
Labelling Requirements for Medical Devices
Dal 12 marzo al 18 giugno 2024
GMP (Good Manufacturing Practices)
/
Soft Skill
Percorso Formativo GMP Project Management