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ENGLISH
ITALIANO
- Archive 2026
Dal 27 febbraio al 22 aprile 2026
Medical Affairs
Medical Affairs Essentials
10, 12 e 17 marzo 2026
GMP (Good Manufacturing Practices)
La Qualifica dei Fornitori GMP
11 e 13 marzo 2026
Medical Device
/
Pharmacovigilance
/
Medical Affairs
/
Medical Writing
/
Clinical Research
La Ricerca della Letteratura Scientifica: dal Quesito ai Risultati
18 marzo 2026
Medical Affairs
/
Clinical Research
Il Consenso è davvero l’unica Base Giuridica per il Trattamento Dati nella Ricerca Clinico-Scientifica?
24 March 2026
Clinical Research
Master the New Swiss Clinical Trial Framework and its Interplay with the EU CTR - Similarities and Differences
25 March 2026
Pharmacovigilance
Attributability and Causality in Pharmacovigilance: Still a Hot Topic
25 e 26 marzo 2026
GMP (Good Manufacturing Practices)
Annex 1 e Contamination Control Strategy
26 and 27 March 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Medical Writing Course: Improve your Writing & Reviewing Skills
08, 10, 15 e 17 aprile 2026
Pharmacovigilance
Il Sistema di Qualità Applicato alla Farmacovigilanza
14 e 16 aprile 2026
Clinical Research
Norme, Novità e Futuro della Ricerca Clinica: Cosa Devi Sapere per Essere Compliant
14 e 15 aprile 2026
Clinical Research
Protezione dei dati personali (GDPR) e Ricerca Scientifica
15 April 2026
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
Advertisement and Promotion Claims for Medical Devices
15 e 17 aprile 2026
Medical Affairs
Il Responsabile del Servizio Scientifico
16 April 2026
GMP (Good Manufacturing Practices)
Introduction to Aseptic Process Simulation (APS)
NEW COURSE
21 e 23 aprile 2026
Regulatory
Integratori Alimentari e Pubblicità: Normativa, Rischi e Strategie di Conformità
21 and 23 April 2026
Regulatory
Fast-Track Your Marketing Authorization Application (MAA): Navigate EU, UK & US Regulatory Pathways with Confidence
07 maggio 2026
Evidence Generation
/
Medical Affairs
/
Clinical Research
Generare Real World Evidence (RWE) con Metodi Osservazionali
07 and 08 May 2026
Pharmacovigilance
Pharmacovigilance Agreements
12 May 2026
Medical Writing
/
Soft Skill
From Data to Impact: Don’t Let Bad Slides Ruin Good Science!
12, 14 e 19 maggio 2026
Medical Affairs
Patient Advocacy ed Engagement in Ambito Farmaceutico ed Healthcare
NEW COURSE
18 and 20 May 2026
Animal Health
/
Regulatory
Veterinary Marketing Authorisation (MAA) and Variations (MAV) in the EU: Regulatory Requirements and Best Practices
19, 20 and 21 May 2026
Medical Affairs
/
Medical Writing
Writing Articles for Peer-Reviewed Journals: Turn Your Research into Published Results
21 and 22 May 2026
Medical Device
/
IVDs (In-Vitro Diagnostics)
/
Regulatory
MDR/IVDR Requirement: The Person Responsible for Regulatory Compliance (PRRC)
26 e 27 maggio 2026
Medical Device
/
Regulatory
I Combination Products ai Sensi del Regolamento UE sui Dispositivi Medici (MDR)
26 e 28 maggio 2026
Clinical Research
La Valutazione di Impatto della Protezione dei Dati (DPIA) nella Ricerca Clinico-Scientifica
28 maggio 2026
Regulatory
Etichettatura degli Integratori Alimentari - Applichiamo la Normativa ad Esempi Reali
09 e 11 giugno 2026
Pharmacovigilance
La Gestione del Case Processing in Farmacovigilanza
10 e 11 giugno 2026
Medical Affairs
Come Pianificare e Condurre Hospital Meeting che Lasciano il Segno
15, 17 and 22 June 2026
Clinical Research
/
Statistics and Data Management
A Practical Guide to Innovative Trial Design
16 and 18 June 2026
Pharmacovigilance
Pharmacovigilance System: Audit & Inspection Readiness
22 June 2026
Regulatory
Food Supplement Regulations in the EU
23, 24 and 25 June 2026
Medical Writing
Tips and Tricks to Improve your Technical/Scientific Writing
01 July 2026
Medical Device
/
Medical Affairs
/
Medical Writing
/
Clinical Research
Writing Science for Lay Audiences
02 July 2026
GMP (Good Manufacturing Practices)
Human Error: the True Root Cause of a Deviation?
TBD
Medical Device
/
Medical Affairs
/
Clinical Research
/
Soft Skill
Oral Presentations
NEW COURSE
TBD
GMP (Good Manufacturing Practices)
Biologics and Biosimilars Manufacturing
TBD
Medical Affairs
/
Regulatory
Codice Deontologico di Farmindustria e le Linee Guida per la Certificazione delle Attività di Informazione Scientifica: come applicarle in Azienda
11 and 12 March 2026
Medical Device
Labelling Requirements for Medical Devices
05 e 06 marzo 2026
Medical Affairs
/
Clinical Research
/
Soft Skill
Dalla Comunicazione Professionale alla Negoziazione
04 and 05 March 2026
Medical Device
/
Medical Writing
Mastering MDCG 2024-3: Comprehensive Training on Clinical Investigation Plans
25 and 26 February 2026
Medical Device
/
Regulatory
Clinical Evaluation for Medical Devices
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