LS Academy - EasyB

23/02/2026

🐾 This comprehensive training provides participants with practical knowledge of , focusing on the operational procedures and regulatory requirements essential for effective drug safety monitoring.
Participants will gain hands-on understanding of reporting obligations, case management workflows, and compliance requirements mandated by regulatory authorities. The training emphasizes real-world application, equipping professionals with the tools and knowledge needed to implement and maintain robust veterinary PV systems within their organizations.

📅 27 May 2026
💻 Online Training
🎓 Camilo Giraldo

Register now 👉 https://lsacademy.com/en/product/veterinary-pharmacovigilance-system-from-compliance-to-safety-excellence/

19/02/2026

🚨 Have you been appointed in your company? This Course is for you.

🗓️Date: 21 - 22 May 2026 | 2 online modules, 6 hours
🎓Trainer: Arkan Zwick, Regulatory Affairs Director

Under EU & , every manufacturer must designate a Person Responsible for Regulatory Compliance (PRRC) - a legally required role with significant responsibilities.

Our course gives you the practical knowledge needed to confidently fulfill PRRC duties and demonstrate compliance.

🎯 Perfect for professionals who have recently taken on, or are about to take on, the PRRC role.

👉 Get prepared for the responsibility your company relies on:
https://lsacademy.com/en/product/person-responsible-for-regulatory-compliance-prrc-an-mdr-ivdr-requirement-3/

Online training on PRRC under MDR & IVDR to master regulatory compliance, role responsibilities and oversight for medical device quality systems.

17/02/2026

🎓 𝗩𝗲𝘁𝗲𝗿𝗶𝗻𝗮𝗿𝘆 𝗠𝗮𝗿𝗸𝗲𝘁𝗶𝗻𝗴 𝗔𝘂𝘁𝗵𝗼𝗿𝗶𝘀𝗮𝘁𝗶𝗼𝗻 (𝗠𝗔𝗔) 𝗮𝗻𝗱 𝗩𝗮𝗿𝗶𝗮𝘁𝗶𝗼𝗻𝘀 (𝗠𝗔𝗩) 𝗶𝗻 𝘁𝗵𝗲 𝗘𝗨: 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗥𝗲𝗾𝘂𝗶𝗿𝗲𝗺𝗲𝗻𝘁𝘀 𝗮𝗻𝗱 𝗕𝗲𝘀𝘁 𝗣𝗿𝗮𝗰𝘁𝗶𝗰𝗲𝘀

📅 18 and 20 May 2026 | online | 02:30-05:30 PM CEST
🧑‍🏫Staša Taferner, PhD

🎯This interactive training course provides a structured approach to understanding the MAA dossier requirements, focusing on clinical and safety documentation, and offers insights into key MAV processes, including Variations Not Requiring Assessment (VNRA) and Variations Requiring Assessment (VRA).

🔗 Discover the programme: https://lsacademy.com/en/product/veterinary-marketing-authorisation-maa-and-variations-mav-in-the-eu-regulatory-requirements-and-best-practices/

11/02/2026

🗣️ Comunicare in modo efficace con medici, farmacisti e altri operatori della salute è un elemento centrale per chi lavora nei settori farmaceutico, dei dispositivi medici, nutraceutico e dell’integrazione alimentare.

🆕 Questo corso offre un percorso strutturato per sviluppare competenze comunicative solide e consapevoli, con un focus sia sugli aspetti tecnici della comunicazione professionale sia sulle dinamiche relazionali che caratterizzano il contesto sanitario.

📅 13 e 14 maggio 2026
📍 Milano

Iscriviti ora 👉 https://lsacademy.com/product/comunicare-efficacemente-con-gli-operatori-della-salute-2/

10/02/2026

🎤2026 LS Academy Conferences - Expand Your Knowledge, Grow Your Network 🌍

🗓German Pharmacovigilance Day | 17 September 2026
10th Anniversary: a Milestone of PV Excellence
https://lnkd.in/dPxuVWqf

🗓MedDev Day | 15 and 16 October 2026
Building Opportunities in the EU Single Market
https://lnkd.in/dfZuVJaQ

🗓Italian Pharmacovigilance Day | 22 ottobre 2026
https://lnkd.in/d9BPvcip

🗓European Statistical Forum | 02 and 03 November 2026
Design and Analysis of Trials in Rare Diseases and Gene Therapies
https://lnkd.in/ddSrNngE

🗓Nordic Pharmacovigilance Day | 11 November 2026
Pharmacovigilance in the Nordics: Innovation, Collaboration, Safety
https://lnkd.in/dmxsPSdV

👉 Don’t miss out – View all details and registration info
https://lnkd.in/dp9H6Cxv

Would you like to become a Sponsor?
📧Get in touch info@lsacademy.com to learn about our tailored sponsorship packages and the exclusive benefits they include.

09/02/2026

🚀 Mastering ISO IDMP: From EU Requirements to Strategic Advantage

European pharmaceutical regulation is evolving fast - and ISO IDMP is no longer optional.

If you work in Regulatory Affairs, Data Management, or Regulatory Operations, understanding how ISO IDMP is implemented in the EU and how it impacts your processes is becoming essential.

📅04 and 06 May 2026 | 2 modules, 6 hours
💻Online Training | Limited Seats

👉 Join us and turn compliance into a competitive advantage
https://lsacademy.com/en/product/mastering-iso-idmp-eu-implementation-and-regulatory-impact/?&utm_source=facebook&utm_medium=social

05/02/2026

📢 Call for Abstracts is Now Open!

European Statistical Forum: Design and Analysis of Trials in Rare Diseases and Gene Therapies
📍 Budapest
📅 02 and 03 November 2026
🧪 Scientific Board : Jens-Otto Andreas Lisa Comarella Fabiola La Gamba

This is the right opportunity to submit an abstract and share your work through a scientific presentation with an international audience of experts.

🔍 Topics of interest include:
• Case studies
• Regulatory experiences
• Statistical challenges and innovations

👉 Download the abstract submission form https://lnkd.in/d_vJbSZ4

👉 Discover more on the conference webpage https://lnkd.in/dXNRay6s

04/02/2026

Take a look at these interesting training opportunities and register now! 🤩

🎓 Effective Management of SAE/SUSAR Reporting and CIOMS Forms
📅 06 May 2026
🧑‍🏫 Marco Anelli, Nicola Sisti
https://lnkd.in/di5KJjMZ

🎓 Pharmacovigilance Agreements
📅07 and 08 May 2026
🧑‍🏫Anna-Shari Melin, Belinda V. Baum
https://lnkd.in/dgmQDBWe

🎓 Advanced Safety Management in Clinical Trials under CTR 536/2014
📅 12 May 2026
👩‍🏫 Elena Prokofyeva
https://lnkd.in/d5t9qqeC

03/02/2026

Generare Real World Evidence (RWE) con Metodi Osservazionali

📅 7 maggio 2026
🕘 dalle ore 09:00 alle 12:00 e dalle 14:30 alle 17:30
⌛ 6 ore di formazione online
👨‍🏫 Giovanni Fiori Celeste Cagnazzo

Questo corso si propone di fornire le basi fondamentali per affrontare con successo la generazione di , con un focus su:

🔹 Il metodo osservazionale e i principali disegni di studio.

🔹 Le normative e le linee guida, con un approfondimento sull’impatto della nuova linea guida .

🔹 Le principali fonti di nell’era della Digital Health.

🔹 Le best practices per organizzare e condurre studi efficaci

Unendo teoria e pratica, il corso offre ai professionisti del settore le competenze necessarie per integrare con successo i RWD nelle strategie di sviluppo e contribuire all’innovazione nella ricerca clinica.

🔥Iscriviti entro il 21 aprile per usufruire della quota scontata Early Bird

👉https://lnkd.in/dim6B4HT

02/02/2026

🆕 NUOVO CORSO | Deviazioni negli Studi Clinici: Riconoscerle, Gestirle, Prevenirle
Dalla teoria alla pratica: strumenti e criteri per una gestione efficace e documentata delle non conformità secondo le nuove GCP R3

🎓 Il corso accompagna i partecipanti passo dopo passo nello sviluppo di una maggiore consapevolezza e capacità di orientamento nella gestione delle deviazioni, con un approccio alla qualità basato sul rischio.

📅 22 Aprile 2026 | dalle ore 14:00 alle 18:00 | online
👩‍🏫 Docente: Carla Polimeni

🔗 Programma ed iscrizioni a questo link:
https://lnkd.in/dZk44V9n

29/01/2026

🎯Do not miss our online training designed to help professionals confidently navigate EU, US, and Canadian cosmetic regulations and bring products to market safely and efficiently.

🗓️05 and 07 May 2026
👥Limited number of participants
🎓Trainer: Claudia Soto, Cosmetic Formulator, Safety Assessor & Regulatory Consultant at Seguridad Cosmética

Ideal for:
🔹professionals managing international product portfolios
🔹those interacting with distributors or global affiliates
🔹professionals who need a high-level, strategic understanding of cosmetic compliance worldwide

👉Secure your place now https://lsacademy.com/en/product/global-cosmetic-compliance-made-simple/?&utm_source=facebook&utm_medium=social

28/01/2026

✨ Make your SSCP clear, compliant, and effective

Join our online course on the Summary of Safety and Clinical Performance (SSCP) and learn how to meet MDR expectations while communicating safety and performance data with confidence.

📅 22 April 2026
🕝 4-hour live online course
🔒 Limited seats

Secure your place now: https://lnkd.in/dFffsNZb

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