LS Academy - EasyB

22/05/2026

𝗖𝗼𝗺𝗽𝘂𝘁𝗲𝗿 𝗦𝘆𝘀𝘁𝗲𝗺 𝗩𝗮𝗹𝗶𝗱𝗮𝘁𝗶𝗼𝗻 (𝗖𝗦𝗩) – 𝗚𝘅𝗣 𝗣𝗿𝗼𝗰𝗲𝘀𝘀 𝗢𝘄𝗻𝗲𝗿 𝗮𝗻𝗱 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲: 𝗜𝗻 𝗼𝗿 𝗢𝘂𝘁?
🎯Contribuire pro-attivamente alla realizzazione di un progetto di convalida di un sistema computerizzato, garantire il mantenimento dello stato di convalida dei sistemi computerizzati e diffondere nella propria realtà l’approccio metodologico che guida l’attività di convalida dei sistemi GxP

📅 08, 12 e 15 giugno 2026 | online
🎓 Docenti: Romina Zanier, Stefano Piccoli
👉 Programma ed iscrizione: https://lsacademy.com/it/product/computer-system-validation-csv-gxp-process-owner-and-quality-assurance-in-or-out-2026/

𝗗𝗮𝘁𝗮 𝗚𝗼𝘃𝗲𝗿𝗻𝗮𝗻𝗰𝗲 𝗲 𝗦𝗶𝘀𝘁𝗲𝗺𝗶 𝗖𝗼𝗺𝗽𝘂𝘁𝗲𝗿𝗶𝘇𝘇𝗮𝘁𝗶 𝗻𝗲𝗴𝗹𝗶 𝗦𝘁𝘂𝗱𝗶 𝗖𝗹𝗶𝗻𝗶𝗰𝗶
🎯Identificare e mappare i sistemi computerizzati che impattano sulla conduzione di uno studio clinico, applicare i principi di data governance lungo l’intero ciclo di vita del dato clinico, valutare il livello di rischio dei sistemi utilizzati e definire il corretto livello di validazione richiesto e strutturare un processo di gestione dei sistemi computerizzati conforme a EMA Guideline e ICH E6(R3)

📅 16 e 19 giugno 2026 | online
🎓 Docente: Laura Monico
👉 Programma ed iscrizione: https://lsacademy.com/it/product/data-governance-e-sistemi-computerizzati-negli-studi-clinici2026/

19/05/2026

📢 𝗖𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲: 𝘂𝗻 𝗥𝘂𝗼𝗹𝗼 𝗖𝗵𝗶𝗮𝘃𝗲 𝗻𝗲𝗹𝗹𝗮 𝗥𝗶𝗰𝗲𝗿𝗰𝗮 𝗖𝗹𝗶𝗻𝗶𝗰𝗮

L’obiettivo del percorso è fornire una preparazione completa e operativa per chi desidera affermarsi nel ruolo di Clinical Quality Assurance Manager o dell’Auditor nell’ambito della ricerca clinica.

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.

Il taglio è fortemente applicativo: i concetti vengono affrontati con un approccio orientato al “saper fare”, grazie anche al coinvolgimento di docenti con esperienza diretta nel settore, che porteranno in aula casi reali e soluzioni concrete.

📅 Dal 25 settembre al 21 novembre 2026
🌐 Modalità: Online
🗣 Lingua: Italiano
👩‍🏫 Docenti: Celeste Cagnazzo Mario Corrado Maurizio Cuocolo Stefano Piccoli Francesca Preite Andrea Pucci Romina Zanier

📌 Posti limitati

🔗 Iscriviti ora e assicurati il tuo posto alla tariffa super early bird:https://lsacademy.com/it/product/clinical-quality-assurance-un-ruolo-chiave-nella-ricerca-clinica-2026/

13/05/2026

🎯Learn how to successfully prepare for PV System audits and inspections conducted by internal QA teams, external parties, or Regulatory Agencies.

𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗼𝘃𝗶𝗴𝗶𝗹𝗮𝗻𝗰𝗲 𝗦𝘆𝘀𝘁𝗲𝗺: 𝗔𝘂𝗱𝗶𝘁 & 𝗜𝗻𝘀𝗽𝗲𝗰𝘁𝗶𝗼𝗻 𝗥𝗲𝗮𝗱𝗶𝗻𝗲𝘀𝘀

📅 16 and 18 June 2026 | 9:30 AM – 12:30 PM CEST | Interactive Zoom sessions
🎓 Trainer: Raj Bhogal
👉 Program: https://lsacademy.com/en/product/pharmacovigilance-system-audit-inspection-readiness-6/

Online training on pharmacovigilance system audit & inspection readiness to master GVP compliance, audit prep and regulatory inspection skills.

22/04/2026

📢 𝐌𝐚𝐬𝐭𝐞𝐫𝐢𝐧𝐠 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐄𝐯𝐚𝐥𝐮𝐚𝐭𝐢𝐨𝐧 𝐮𝐧𝐝𝐞𝐫 𝐌𝐃𝐑 - 𝐉𝐨𝐢𝐧 𝐮𝐬 𝐭𝐡𝐢𝐬 𝐒𝐞𝐩𝐭𝐞𝐦𝐛𝐞𝐫

In today’s regulatory landscape, writing a robust Clinical Evaluation Plan (CEP) and Clinical Evaluation Report (CER) is no longer optional, it’s essential.

This interactive online training will guide you step-by-step through the full clinical evaluation process, aligned with MDR 2017/745 requirements.

🔍 𝐖𝐡𝐚𝐭 𝐲𝐨𝐮’𝐥𝐥 𝐠𝐚𝐢𝐧:
🔹A clear understanding of how to develop an effective CEP
🔹Practical tools to perform and structure clinical literature reviews
🔹Hands-on insights into writing a compliant CER
🔹A deeper approach to benefit-risk analysis and post-market surveillance

📅 16, 17 and 21 September 2026
💻 Live online training
🎓 Trainer: Gillian Pritchard, Director, Sylexis Limited

Ready to strengthen your expertise and stay ahead in MDR compliance?

👉 Discover more and secure your spot: https://lsacademy.com/en/product/how-to-write-a-clinical-evaluation-plan-and-report-6/

Online training on how to write a clinical evaluation plan and report to master structure, compliance and practical regulatory documentation skills.

21/04/2026

𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗼𝘃𝗶𝗴𝗶𝗹𝗮𝗻𝗰𝗲 𝗗𝗼𝗰𝘂𝗺𝗲𝗻𝘁𝘀 𝗶𝗻 𝘁𝗵𝗲 𝗟𝗶𝗳𝗲 𝗖𝘆𝗰𝗹𝗲 𝗼𝗳 𝗮 𝗠𝗲𝗱𝗶𝗰𝗶𝗻𝗮𝗹 𝗣𝗿𝗼𝗱𝘂𝗰𝘁

💡This 6-module (24 hours total) highly interactive online training path is intended for professionals involved in the planning, preparation, coordination, and review of aggregated safety reports. It is designed to provide an extensive overview of pharmacovigilance activities and related documents throughout the life cycle of a medicinal product.

At the end you will be able to:
✔ Understand the main pharmacovigilance activities in the life cycle of the medicinal product
✔ Plan and prepare DSUR, PSUR/PBRER, RMP, and AddCO, exploiting similarities and synergies among the different documents
✔ Apply writing skills to the preparation of pharmacovigilance documents

👉 Discover more https://lsacademy.com/en/product/pharmacovigilance-documents-in-the-life-cycle-of-a-medicinal-product-2026/

10/04/2026

𝐆𝐨𝐨𝐝 𝐃𝐢𝐬𝐭𝐫𝐢𝐛𝐮𝐭𝐢𝐨𝐧 𝐏𝐫𝐚𝐜𝐭𝐢𝐜𝐞𝐬 (𝐆𝐃𝐏) 𝐟𝐨𝐫 𝐌𝐞𝐝𝐢𝐜𝐢𝐧𝐞𝐬 𝐚𝐧𝐝 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐃𝐞𝐯𝐢𝐜𝐞𝐬
𝘍𝘳𝘰𝘮 𝘳𝘦𝘨𝘶𝘭𝘢𝘵𝘰𝘳𝘺 𝘳𝘦𝘲𝘶𝘪𝘳𝘦𝘮𝘦𝘯𝘵𝘴 𝘵𝘰 𝘳𝘦𝘢𝘭-𝘸𝘰𝘳𝘭𝘥 𝘪𝘮𝘱𝘭𝘦𝘮𝘦𝘯𝘵𝘢𝘵𝘪𝘰𝘯

Join our upcoming online training course, designed to provide a practical and inspection-oriented understanding of GDP requirements.

📅 07 and 09 July 2026
🕘 9:00 AM – 1:00 PM (CEST) | Online
👩‍🏫 New Trainer: Maria Àngels Moral, Deputy Responsible Person, SAIMA Global Farma

𝐆𝐚𝐢𝐧 𝐚 𝐩𝐫𝐚𝐜𝐭𝐢𝐜𝐚𝐥, 𝐢𝐧𝐬𝐩𝐞𝐜𝐭𝐢𝐨𝐧-𝐫𝐞𝐚𝐝𝐲 𝐮𝐧𝐝𝐞𝐫𝐬𝐭𝐚𝐧𝐝𝐢𝐧𝐠 𝐨𝐟 𝐆𝐃𝐏 𝐫𝐞𝐪𝐮𝐢𝐫𝐞𝐦𝐞𝐧𝐭𝐬 𝐚𝐧𝐝 𝐥𝐞𝐚𝐫𝐧 𝐡𝐨𝐰 𝐭𝐨 𝐚𝐩𝐩𝐥𝐲 𝐭𝐡𝐞𝐦 𝐞𝐟𝐟𝐞𝐜𝐭𝐢𝐯𝐞𝐥𝐲 𝐚𝐜𝐫𝐨𝐬𝐬:
✔ Warehousing
✔ Transport
✔ Outsourced activities

🎯 Ideal for professionals in quality, logistics, and regulatory roles
👉 Join us and strengthen your GDP compliance
https://lsacademy.com/en/product/good-distribution-practices-gdp-for-medicines-and-medical-devices/

Practical online training on Good Distribution Practices (GDP) for medicines & medical devices with regulatory insights and operational compliance guidance.

09/04/2026

🚀 𝐒𝐭𝐫𝐞𝐧𝐠𝐭𝐡𝐞𝐧 𝐲𝐨𝐮𝐫 𝐌𝐃𝐑 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐒𝐭𝐫𝐚𝐭𝐞𝐠𝐲

Navigating the evolving landscape of the EU is no longer optional, it’s a strategic priority.

That’s why we’re bringing together two of our successful trainings to help professionals build solid, compliant, and future-proof clinical documentation 👇

🔹 𝐒𝐮𝐦𝐦𝐚𝐫𝐲 𝐨𝐟 𝐒𝐚𝐟𝐞𝐭𝐲 𝐚𝐧𝐝 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐏𝐞𝐫𝐟𝐨𝐫𝐦𝐚𝐧𝐜𝐞
Master how to create clear, compliant, and effective SSCP documents
🎓Trainer: Geneviève Laumen, Medical Writer
👉 https://lsacademy.com/en/product/summary-of-safety-and-clinical-performance-sscp/

🔹 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐄𝐯𝐚𝐥𝐮𝐚𝐭𝐢𝐨𝐧 𝐟𝐨𝐫 𝐌𝐞𝐝𝐢𝐜𝐚𝐥 𝐃𝐞𝐯𝐢𝐜𝐞𝐬
Learn how to develop solid clinical evidence and meet MDR requirements
🎓Trainer: Arkan Zwick, Regulatory Affairs Director
👉 https://lsacademy.com/en/product/clinical-evaluation-for-medical-devices-8/

08/04/2026

🎯 The goal of this online training is to develop participants’ capability to prepare high-quality, scientifically sound, and regulatory-compliant safety narratives that meet the expectations outlined in Post-approval safety data management ICH E2D, Electronic transmission of individual case safety reports (ICSRs) ICH E2B(R3) and relevant GVP guidance.

🗓️30 June 2026 from 2:00 pm to 6:00 pm CEST
🎓 Liana Kasyan

Register now 👉 https://lsacademy.com/en/product/narrative-writing-in-pharmacovigilance-ensuring-clarity-consistency-and-regulatory-readiness-in-line-with-ich-e2d-e2br3-and-gvp-principles/

Online training on narrative writing in pharmacovigilance to master clarity, consistency and regulatory readiness with ICH E2D/E2BR3 and GVP principles.

25/03/2026

𝗙𝗼𝗼𝗱 𝗦𝘂𝗽𝗽𝗹𝗲𝗺𝗲𝗻𝘁 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗶𝗼𝗻𝘀 𝗶𝗻 𝘁𝗵𝗲 𝗘𝗨

💡 This course gives a clear and practical overview of the EU rules for food supplements. Participants will learn about regulatory requirements, including compliance, labeling, and rules on health claims.

We will also compare EU, US, and Canadian rules, helping participants understand key differences and best practices.

🗓️ 22 June 2026 | Online
🎓 Enej Šterbenc, Lara Šterbenc from Billev Pharma East Ltd.

Register now 👉 https://lsacademy.com/en/product/food-supplement-regulations-in-the-eu-2026/

Online training on EU food supplement regulations 2026 to master compliance, safety, labeling and best regulatory practices across the EU.

24/03/2026

❓ What are the characteristics of good quality technical/scientific documents?
❓ How can we prepare documents that please our audience?
❓ Are there general rules that might help us effectively write any type of technical/scientific documents?

This course will answer those questions and more, putting you on the right path to become a skilled and successful writer. Through exercises and discussion, you will learn fundamental techniques that will allow you to prepare high quality documents.

🗓️ 23, 24 and 25 June 2026
🎓 Fiona Dunlevy

Register now 👉 https://lsacademy.com/en/product/tips-and-tricks-to-improve-your-technical-scientific-writing-6/

Online course to improve your technical and scientific writing with practical guidance for clarity, precision and publication success.