LS Academy - EasyB

11/08/2025

Welcome to Pharma IT as Platinum Sponsor at the Nordic Pharmacovigilance Day 2025!
Discover more on the website: https://lsacademy.com/en/product/nordic-pharmacovigilance-day-6/

07/08/2025

📣 2025 is the must-attend event for anyone navigating the evolving landscape of global regulation.

Join us in Budapest on 13–14 October 2025 for one and a half days of insights, networking, and strategies.

🎯 Shifting Mindsets: The Future of Global Medical Device Regulation - How regulatory changes are reshaping global business strategies

AGENDA HIGHLIGHTS
📌Regional Regulatory Updates: Japan, China, MEA & EAEU
📌Workshop: AI in Regulatory Affairs – Buzzword or Game-Changer?
📌EU Regulatory Deep Dive – from MDR challenges to high-risk devices
📌Clinical Data & RWE – real-world evidence, surveys, PMCF, and more
📌Regulatory Strategy in Practice – including global clinical data use
🧑‍🤝‍🧑 Dedicated networking lunch & interactive workshops

With insights from leaders at MedTech Europe, CE Certiso, Purdie Pascoe, BSI, AKRA Team, MECOMED, 3Aware, HOYA Surgical Optics, Edwards Lifesciences, and more, this 7th edition brings clarity to complexity.

👉💰Secure your spot before September 15th at the Early Bird fee
https://lsacademy.com/en/product/meddev-day-2025-shifting-mindsets/

Join MedDev Day 2025 in Budapest to explore Shifting Mindsets, global regulatory updates, AI, and shape the future of medical devices.

06/08/2025

💻 Veterinary QPPV Oversight – Online Training
🗓 29 September 2025 | ⏰ 4 hours | 🎓 Certificate of attendance

Ensure full compliance with Regulation (EU) 2019/6 and VGVP guidelines!
Learn best practices for Veterinary QPPV oversight, QMS, and pharmacovigilance processes.

👨‍🏫 Trainer: Klemen Rojnik, MPharm - Medical and QA manager at Billev Pharma East Ltd.

🔒 Limited Seats – register now https://lsacademy.com/en/product/veterinary-qppv-oversight-systems-and-processes-to-comply-with-the-vmp-regulation-and-vgvp/

The Qualified Person for Pharmacovigilance (QPPV) in the veterinary field is responsible for ensuring the continuous monitoring of the safety of veterinary medicinal products (VMPs). They oversee the collection, assessment, and reporting of adverse events, ensuring compliance with regulatory require...

05/08/2025

Accurate data collection is the essential starting point of the vast process of . During this crucial phase, it is vital to evaluate various data sources, each with its own strengths and limitations. At the same time, it is crucial to monitor the practical implementation of signals and ensure that the entire critical process fully meets regulatory expectations.

💡 This course provides participants the opportunity to gain a comprehensive and in-depth understanding of signal investigation and management.

📆 23, 25 and 30 September 2025
💻 9 hours online training
🎓 Francesco Tescione

Register now 👉 https://lsacademy.com/en/product/signal-detection-and-signal-management/

04/08/2025

𝗦𝗲𝗹𝗲𝘇𝗶𝗼𝗻𝗲 𝗲 𝗖𝗼𝗻𝘃𝗮𝗹𝗶𝗱𝗮 𝗱𝗶 𝗨𝗻𝗮 𝗦𝗼𝗹𝘂𝘇𝗶𝗼𝗻𝗲 𝗖𝗹𝗼𝘂𝗱 𝗶𝗻 𝗔𝗺𝗯𝗶𝘁𝗼 𝗚𝘅𝗣
📅07, 09, 14 e 16 ottobre 2025 | Online | h.09:00/13:00 | 16 ore di formazione
🎓 Docente: Laura Monico

🎯 il corso, si propone di fornire una panoramica delle diverse fasi di adozione del modello Cloud: dalla selezione del fornitore, alla convalida della soluzione prescelta, alle attività e ai processi di gestione della soluzione nella fase operativa fino alla chiusura del rapporto con il fornitore stesso.
Nel corso saranno presentate le basi della terminologia e dei modelli di implementazione del cloud, inclusi SaaS, PaaS e IaaS.

Per info e iscrizioni 👉

In un ambiente informatico in continua evoluzione tecnologica, l’utilizzo di soluzioni Cloud e SaaS (Software as a Service) è in costante crescita anche nel mondo “regolato” delle Life Sciences. Sebbene adottare una soluzione Cloud/SaaS possa essere una opzione che risponde in modo eccellente...

01/08/2025

🌞 Happy Summer from LS Academy Team! 🌞

As we step into August, we want to wish all our lovely clients, partners and followers a joyful and restorative Summer ⛱️🏕️🎡

Take this time to breathe and relax... and then, come back ready to grow and learn! September is just around the corner 😉 We will be here, ready to support your journey 🚀

https://lsacademy.com/en/

28/07/2025

Stai cercando una formazione concreta e spendibile nel settore della ricerca clinica?

Il nostro percorso formativo 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲: 𝘂𝗻 𝗥𝘂𝗼𝗹𝗼 𝗖𝗵𝗶𝗮𝘃𝗲 𝗻𝗲𝗹𝗹𝗮 𝗥𝗶𝗰𝗲𝗿𝗰𝗮 𝗖𝗹𝗶𝗻𝗶𝗰𝗮 nasce proprio per questo: formare professionisti in grado di progettare, implementare e mantenere un sistema qualità efficace e conforme alle normative.

🗓️ dal 26 settembre al 22 novembre 2025 | online | formula weekend
🕒 Attraverso un programma strutturato di 61,5 ore, il corso accompagna i partecipanti in un viaggio formativo che parte dalle basi normative fino ad arrivare agli strumenti più pratici per la gestione del sistema qualità, la conduzione degli audit, la preparazione alle ispezioni e l’analisi delle non conformità.

✔️ Solida base normativa
✔️ Strumenti pratici per audit, ispezioni e gestione documentale
✔️ Docenti con esperienza diretta nel settore
✔️ Casi reali e approccio applicativo orientato al “saper fare”

🎓Celeste Cagnazzo Mario Corrado Maurizio Cuocolo Stefano Piccoli Francesca Preite Andrea Pucci Antonella Ursini Romina Zanier

👉 visita il sito per maggiori dettagli https://lsacademy.com/product/clinical-quality-assurance-un-ruolo-chiave-nella-ricerca-clinica-4/

❗ Posti limitati
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24/07/2025

🚨 𝐿𝑎𝑠𝑡 𝑠𝑒𝑎𝑡𝑠 𝑎𝑣𝑎𝑖𝑙𝑎𝑏𝑙𝑒! 🚨
𝐎𝐧𝐥𝐢𝐧𝐞 𝐓𝐫𝐚𝐢𝐧𝐢𝐧𝐠 – 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐃𝐞𝐯𝐢𝐜𝐞𝐬
𝐇𝐨𝐰 𝐭𝐨 𝐖𝐫𝐢𝐭𝐞 𝐚 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐄𝐯𝐚𝐥𝐮𝐚𝐭𝐢𝐨𝐧 𝐏𝐥𝐚𝐧 𝐚𝐧𝐝 𝐑𝐞𝐩𝐨𝐫𝐭

📅 17, 18 and 22 September 2025
🕒 9 hours | 🌐 Online
Learn how to create a compliant CEP and CER under MDR 2017/745, including literature review, PMS, and benefit-risk assessment.

📌 Limited spots – book now!
🔗 https://lsacademy.com/en/product/how-to-write-a-clinical-evaluation-plan-and-report-5/

21/07/2025

𝗗𝗲𝗰𝗼𝗱𝗶𝗻𝗴 𝗘𝗹𝗲𝗰𝘁𝗿𝗼𝗻𝗶𝗰 𝗣𝗿𝗼𝗱𝘂𝗰𝘁 𝗜𝗻𝗳𝗼𝗿𝗺𝗮𝘁𝗶𝗼𝗻 (𝗲𝗣𝗜)

🗓 26 November 2025 | Online | 2:00/6:00 pm CET
🎓 Munnik

At the end of the training, you will be able to:

✅Have an overview of the latest developments in ePI
✅Understand the electronic data exchange standard (FHIR)
✅Understand how effective data management will help an organization/department to meet the requirements of EMA for ePI

Discover more 👉https://lsacademy.com/en/product/decoding-electronic-product-information-epi-2/

16/07/2025

𝗧𝗵𝗲 “𝗚𝗹𝗼𝗯𝗮𝗹” 𝗤𝘂𝗮𝗹𝗶𝗳𝗶𝗲𝗱 𝗣𝗲𝗿𝘀𝗼𝗻 𝗥𝗲𝘀𝗽𝗼𝗻𝘀𝗶𝗯𝗹𝗲 𝗳𝗼𝗿 𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗼𝘃𝗶𝗴𝗶𝗹𝗮𝗻𝗰𝗲 (𝗤𝗣𝗣𝗩) 𝗪𝗼𝗿𝗸𝘀𝗵𝗼𝗽

🗓 22 September 2025 | Online | 02:00/06:00 pm CEST
🎓 Ilaria Grisoni Colombo

Unlock the knowledge you need to:
🎯Understand the evolution of the role and responsibilities of the QPPV, including oversight of the pharmacovigilance system.
🎯Learn about global regulatory requirements and guidelines related to QPPV.
🎯Establish a robust and effective QPPV oversight process, including delegation of task, maintenance of the PSMF, and quality management.
🎯Prepare for inspection/audit as a QPPV, based on the PV inspection types
Discover more 👉 https://lsacademy.com/en/product/the-global-qualified-person-responsible-for-pharmacovigilance-qppv-workshop-2025/

14/07/2025

🆕 Technology Transfer Farmaceutico

Questo corso ha l’obiettivo di fornire una visione chiara e operativa del , guidando i partecipanti attraverso le sue fasi principali con un approccio pratico, attraverso la presentazione e discussione di case studies reali e momenti di confronto diretto con il docente, per favorire l’applicazione concreta dei concetti appresi.

📆 20, 23 e 27 ottobre 2025
💻 9 ore di formazione online
🎓 Roberto Giannoccaro

Iscriviti subito alla tariffa scontata Early Bird 👉 https://lsacademy.com/product/technology-transfer-farmaceutico/

10/07/2025

💥 We are proud to announce that the FINAL AGENDA of the Nordic Pharmacovigilance Day has been released!

Take a look at the programme here 👉 https://lsacademy.com/en/product/nordic-pharmacovigilance-day-6/program

See you in Copenhagen on November 11th, 2025 🤩