ASPHALION KNOWLEDGE CENTRE | Advanced training on the Clinical Trials Information System (CTIS)

Welcome to Asphalion Knowledge Centre, a training platform for Biotech, Pharma and MedTech professionals. Our platform offers specialized courses taught by expert trainers familiar with EU and US regulations, ensuring a relevant learning experience.

Welcome to Asphalion Knowledge Centre, a training platform for Biotech, Pharma and MedTech professionals. Our platform offers specialized courses taught by expert trainers familiar with EU and US regulations, ensuring a relevant learning experience.
June 14, 2024

Register for our next Asphalion Knowledge Centre course, Advanced training on the Clinical Trials Information System (CTIS)!

When? New Date!! September 17

Where? Online

The Regulation (EU) No 536/2014 establishes that clinical trials in the European Union must be managed through the Clinical Trials Information System (CTIS). The Regulation came into force in January 2022, providing a 3-year transition period until January 2025.

This course provides key guidance for the successful implementation and management of the CTIS portal from the initial clinical trial application throughout its life-cycle, as well as a live demonstration of the main functionalities of the system.

CHECK OUT THE COMPLETE AGENDA HERE

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If you have any questions, you can contact us at: [email protected]

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EVENTS | Asphalion present at Key events this year

At Asphalion, we’re excited to be part of key events, conferences, and summits throughout 2026—great opportunities to connect, exchange insights, and collaborate with leaders across healthcare and medical devices. 

EVENT | DIA Europe

DIA Europe 2026 will take place in Rotterdam from 24–26 March 2026. As Europe’s largest neutral conference in the life sciences sector, it will gather 1,500 professionals from over 50 countries for three days of exchange and collaboration. The programme features 10 dynamic tracks covering key areas such as Clinical Trials Innovation, AI & Real-World Evidence, Innovative Therapies, Medical Devices, and Pharmacovigilance, alongside 80+ sessions and contributions from 300+ experts, regulatory authorities, HTA bodies, payers, and patient organizations—offering a key platform to drive innovation and informed decision-making in healthcare.

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