Please register for this webinar here.

SPARK The Midlands are very fortunate to have DLRC deliver back-to-back webinars for us. This second one is an introduction to the EU Clinical Trials Regulation (EU-CTR), designed to support sponsors in navigating the new regulatory landscape. This session will provide an overview of the key changes introduced by EU-CTR, guidance on using Clinical Trials Information System (CTIS) and insights into preparing compliant submissions across member states. Whether you're new to clinical trials or looking to refresh your understanding, this training offers a concise, hands-on look at what you need to know to submit successful applications under the new framework.

Hosted by Christie Watson, a Regulatory Affairs professional with seven years of experience with both local and global regulatory submission management, specialising in clinical drug development. She began her career at a CRO, gaining broad exposure to a wide range of therapeutic areas, working with both small molecules and biologics. ​Since joining DLRC in 2021, Christie has played a key role in supporting clients through the preparation and submission of Clinical Trial Applications (CTAs) across the UK, EU and RoW markets.

Join us in learning more about the regulatory landscape for therapeutics in the EU.