EORTC Prepares to Show How to Navigate Regulatory Triangle
How can you navigate the regulatory triangle safely?
How can you navigate the regulatory triangle safely? Who better to address this question than the respected Brussels-based European Organization for Research and Treatment of Cancer (EORTC).
For anybody seeking regulatory tips and tricks on clinical trials, in vitro diagnostics and data protection, EORTC is staging a workshop in Brussels on 2 December. During the same week, it is organizing two-day meetings about innovation and biomarkers in cancer drug development and markers in cancer diagnostic development.
Among its partners in these events are the European Medicines Agency, the National Cancer Institute, the American Association for Cancer Research, and the American Society of Clinical Oncology.
The EORTC is an independent research organization dedicated to investigator driven clinical trials and translational research. Consisting of both a network and a coordinating scientific and operational infrastructure, it seeks to not only establish ‘state-of-the-art’ treatments but also ensure that new cancer agents are developed and tested efficiently with the aim of minimizing delays between laboratory discovery and their therapeutic benefit for patients.
Unlock Commercial Growth through Data-Driven Patient and HCP Insights
May 2nd 2025Leveraging data-driven patient and healthcare provider (HCP) insights, including social drivers of health (SDOH), is essential for life sciences companies to continuously improve patient engagement and commercial success. Mark Rodgers, AVP of Commercial Analytics at Inovalon, discusses how identifying treatment milestones, assessing HCP performance, and segmenting patient populations using SDOH data can drive targeted strategies that improve healthcare outcomes and market access
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
FDA Approves Nipocalimab for the Treatment of Generalized Myasthenia Gravis
April 30th 2025Approval is based on results from the pivotal Vivacity-MG3 trial in which IMAAVY (nipocalimab-aahu) demonstrated superior disease control throughout 24 weeks when compared to placebo plus standard of care.
