+39.035.515.684
info@lsacademy.com
Newsletter
Login or register
0
No products in the cart.
0
No products in the cart.
About Us
Training
Training
Training Paths
Conferences
Medical Writing
Services
Blog
Contacts
ENGLISH
ITALIANO
Courses - Archivio 2024
13 dicembre 2024
Clinical Research
ICH GCP (R3)
10 and 12 December 2024
Animal Health
/
Pharmacovigilance
Introduction to Veterinary Pharmacovigilance
03 December 2024
Animal Health
/
Pharmacovigilance
Veterinary Pharmacovigilance Quality Management
19, 21, 26 and 28 November 2024
GMP (Good Manufacturing Practices)
Computer System Validation (CSV) and Assurance (CSA)
28 November 2024
Pharmacovigilance
The “Global” Qualified Person Responsible for Pharmacovigilance (QPPV) Workshop
27 November 2024
Animal Health
/
Regulatory
Veterinary Marketing Authorisation Variation (MAV) in the EU
26 and 27 November 2024
Medical Device
/
Medical Affairs
/
Clinical Research
Medical Reading
20 and 25 November 2024
Evidence Generation
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Protocol Writing and Communication of Real World Evidence
25 November 2024
GMP (Good Manufacturing Practices)
GMP Inspections: How to Be Ready?
19 and 21 November 2024
Pharmacovigilance
Mastering Benefit Risk Assessment in Pharmacovigilance
19 and 21 November 2024
Pharmacovigilance
Pharmacovigilance Quality Management System (QMS)
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
20 November 2024
Regulatory
Decoding Electronic Product Information (ePI)
11, 15 e 18 novembre 2024
Clinical Research
Audit to Computer Systems
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)
12 e 14 novembre 2024
Medical Device
/
Regulatory
La Vigilanza Post Market per i Dispositivi Medici secondo MDR e FDA
12 and 14 November 2024
GMP (Good Manufacturing Practices)
Sterilization Validation
05, 07, 12 e 14 novembre 2024
Pharmacovigilance
/
Clinical Research
Safety Management e Farmacovigilanza
06, 08 e 13 novembre 2024
Regulatory
Integratori Alimentari - Aspetti Tecnico-Regolatori e Panorama Normativo
05 and 07 November 2024
Regulatory
Marketing Authorization Application in EU, US and UK
05 and 07 November 2024
Pharmacovigilance
/
Medical Affairs
/
Clinical Research
Beyond PubMed
30 October and 06 November 2024
GMP (Good Manufacturing Practices)
/
Regulatory
Advanced Therapy Medicinal Product (ATMP): a Roadmap from Classification to Regulation and Manufacturing
04 novembre 2024
GMP (Good Manufacturing Practices)
La Compliance ai Requisiti GMP: Ruolo e Funzioni dell’Assicurazione Qualità
29 and 31 October 2024
GMP (Good Manufacturing Practices)
Cleaning Validation
31 ottobre 2024
Medical Device
/
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Ricerca della Letteratura Scientifica: come Sfruttare le Risorse Gratuite in Rete
30 October 2024
Animal Health
/
Regulatory
Veterinary Marketing Authorisation Application (MAA) in the EU
29 October 2024
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Writing Science for Lay Audiences
28 and 29 October 2024
Medical Device
Initiating the Development of Artificial Intelligence (AI) Medical Devices
22 e 29 ottobre 2024
Regulatory
Terapie Geniche e Terapie Cellulari
21 e 24 ottobre 2024
Medical Affairs
/
Clinical Research
Terapie Digitali (DTx): a che Punto Siamo?
23 and 24 October 2024
Medical Writing
/
Clinical Research
Clinical Study Reports – a 360° Perspective
15 e 23 ottobre 2024
Medical Affairs
/
Regulatory
/
Clinical Research
Off-Label, Uso Compassionevole e Accesso Precoce (Early Access)
22 and 23 October 2024
Animal Health
/
Pharmacovigilance
Veterinary Pharmacovigilance System
23 October 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on Addendum to the Clinical Overview (AddCO) and Referrals
22 October 2024
Medical Device
What You Need to Know about Medical Device Software and Never Dared to Ask
17 October 2024
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Soft Skill
How to Create Effective Visuals for Better Communicating your Science
09 October and 16 October 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents – Focus on the Periodic Safety Update Report (PSUR)
15 and 16 October 2024
Medical Device
Medical Devices Periodic Safety Update Report (PSUR)
17 October 2024
GMP (Good Manufacturing Practices)
Human Error: the True Root Cause of a Deviation?
10 and 11 October 2024
Medical Device
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
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
21 and 28 October 2024
GMP (Good Manufacturing Practices)
Biologics and Biosimilars Manufacturing
01 e 03 ottobre 2024
Regulatory
Cosmetici - Aspetti Tecnico-Regolatori e Panorama Normativo
02 October 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on the Risk Management Plan (RMP)
02 October 2024
Regulatory
Electronic Submissions and Data Management in Regulatory Affairs
15 and 17 October 2024
Regulatory
The Basics of Regulatory Affairs for Cosmetic Products in US and Canada
09 ottobre 2024
Regulatory
Integratori Alimentari ed Advertising
15 October 2024
GMP (Good Manufacturing Practices)
Introduction to Aseptic Process Simulation (APS)
26 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 e 26 settembre 2024
Medical Device
ISO 14155/2020 - Come Svolgere uno Studio Clinico con Dispositivi Medici
23 and 26 September 2024
Medical Device
/
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Searching the Medical Literature
25 September 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Focus on Signal Management and Development Safety Update Reports (DSUR)
STEP 2 : 10 and 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
10 and 11 October 2024
Medical Device
/
Regulatory
US FDA 101 - Fundamentals of Pre-market Submissions to CDRH
23 e 24 settembre 2024
Medical Device
/
Regulatory
La Biocompatibilità e la Caratterizzazione Chimica: Dispositivi Medici Sicuri
24 e 26 settembre 2024
Medical Device
/
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Ricerca della Letteratura Scientifica: dal Quesito ai Risultati
16, 19 and 23 September 2024
Pharmacovigilance
/
Regulatory
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
08 e 10 ottobre 2024
Regulatory
Gestione della Proprietà Industriale - Il Brevetto per Tutelare le Invenzioni
27 settembre 2024
Medical Affairs
/
Regulatory
Codice Deontologico di Farmindustria e le Linee Guida per la Certificazione delle Attività Scientifiche: come applicarle in azienda
20 settembre 2024
GMP (Good Manufacturing Practices)
ICH Q9 Quality Risk Management
19 e 20 settembre 2024
IVDs (In-Vitro Diagnostics)
/
Clinical Research
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 (Good Manufacturing Practices)
EU GMP Annex 15 - La Qualifica e la Convalida nell'Industria Farmaceutica
18 September 2024
Pharmacovigilance
/
Medical Writing
Pharmacovigilance Documents - Basic Concepts and Definitions for Pharmacovigilance Writing
01 and 02 October 2024
GMP (Good Manufacturing Practices)
Process Validation
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
16 September 2024
GMP (Good Manufacturing Practices)
Quality by Design
17 and 18 September 2024
Pharmacovigilance
Introduction to Pharmacovigilance
17 September 2024
Animal Health
/
Regulatory
Good Distribution Practices (GDP) for Veterinary Medicinal Products
16 and 17 July 2024
Medical Device
/
Regulatory
/
Clinical Research
Good Distribution Practices of Medical Devices
25 e 27 giugno, 2 e 4 luglio 2024
Clinical Research
Selezione e Convalida di Una Soluzione Cloud in Ambito GxP
02 July 2024
GMP (Good Manufacturing Practices)
Statistical Process Control for Pharmaceutical Manufacturing
28 giugno 2024
Clinical Research
Qualifica dei Vendor nella Ricerca Clinica - Approfondimenti
18, 24 and 27 June 2024
Clinical Research
/
Statistics and Data Management
A Practical Guide to Innovative Trial Design
26 giugno 2024
Regulatory
Integratori Alimentari e Advertising: Applichiamo la Teoria alla Pratica
14 and 21 June 2024
Pharmacovigilance
The PSMF (Pharmacovigilance System Master File): from GVPs to Inspections
18 and 20 June 2024
Regulatory
Fundamentals of European Cosmetics Regulatory Affairs
18 and 20 June 2024
Pharmacovigilance
Pharmacovigilance System: Audit & Inspection Readiness
19 and 20 June 2024
Medical Device
/
Regulatory
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
Regulatory
/
Clinical Research
Computer System Validation (CSV) - GxP Process Owner and Quality Assurance: In or Out?
25 and 26 June 2024
Animal Health
/
Pharmacovigilance
Reporting Requirements in Veterinary Pharmacovigilance
02 and 03 July 2024
Medical Device
Labelling Requirements for Medical Devices
06, 07, 12 e 14 giugno 2024
Pharmacovigilance
Il Sistema di Qualità Applicato alla Farmacovigilanza
04, 06 e 11 giugno 2024
Pharmacovigilance
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
Pharmacovigilance
La Gestione del Case Processing in Farmacovigilanza
04 e 06 giugno 2024
Clinical Research
General Data Protection Regulation (GDPR), Ricerca Scientifica e Norme Locali
28 e 30 maggio 2024
Medical Affairs
Il Responsabile del Servizio Scientifico
27 May 2024
Soft Skill
Oral Presentations
21, 24 and 28 May 2024
Pharmacovigilance
/
Regulatory
Pharmacovigilance and Safety in Clinical Trials under the Clinical Trial Regulation (EU) No 536/2014
11 giugno 2024
GMP (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
Pharmacovigilance
/
Market Access
/
Medical Affairs
/
Regulatory
Patient Support Program (PSP) e Compliance: quali Normative Considerare?
22 maggio 2024
Regulatory
Etichettatura degli Integratori Alimentari - Applichiamo la Normativa ad Esempi Reali
21 and 22 May 2024
Pharmacovigilance
Pharmacovigilance Agreements
14, 16 e 21 maggio 2024
Medical Affairs
Patient Advocacy ed Engagement nell’Azienda Farmaceutica
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
16 and 17 May 2024
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Person Responsible for Regulatory Compliance (PRRC) - An MDR/IVDR Requirement
13, 15 and 16 May 2024
Medical Device
How to Write a Clinical Evaluation Plan and Report
07 e 09 maggio 2024
Regulatory
La Pubblicità del Farmaco
08 maggio 2024
Medical Affairs
Progettare e Comunicare in Medical Affairs
15 e 16 maggio 2024
IVDs (In-Vitro Diagnostics)
La Sorveglianza Post-Market dei Dispositivi Diagnostici in Vitro
22 May 2024
Soft Skill
Beyond Slide Decks
29 April 2024
Medical Device
From Good to Excellent: The Summary of Safety and Clinical Performance (SSCP)
23 aprile 2024
Medical Affairs
Progettare un Patient Support Program (PSP): Configurazione del Processo e Strumenti
23 April 2024
Medical Device
Select the Ideal PMCF Strategy for a Medical Device
09 e 10 maggio 2024
GMP (Good Manufacturing Practices)
Agile Project Management: Gestire l’Innovazione nel Contesto della Produzione Farmaceutica
16 e 18 aprile 2024
Clinical Research
Normativa della Ricerca Clinica tra Presente e Futuro
18 April 2024
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Medical Affairs
/
Regulatory
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
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
10 aprile 2024
Medical Affairs
/
Regulatory
/
Clinical Research
I Radiofarmaci
03 e 05 aprile 2024
GMP (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 (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
20, 21 and 25 March 2024
Medical Device
How to Write a Clinical Evaluation Plan and Report
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
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
TBD
Market Access
Healthcare Modeling: Interventi per Migliorare Efficacia ed Efficienza delle Cure
TBD
Market Access
Clinical Support Programs: Strategie e Progetti per Favorire le Attività degli HCP
