The considerable uncertainty caused by Brexit is proving a goldmine for conference organizers, it seems. The Drug Information Association (DIA) is the latest group to put together a meeting about this hot topic.
“Brexit will have a considerable impact on the regulation and supply of medicines to patients,” noted the DIA in a statement. “With the time frame for Brexit fast elapsing, governments, regulators, companies, healthcare systems, and patients are all seeking to prepare for the “known unknowns” and to brace for the “unknown unknowns”. However, information is scarce and not always accessible or confirmed.”
At its meeting to be held in London on December 8, DIA plans to bring stakeholders together to share their knowledge about operational and strategic measures being taken to prevent or minimize the impact of Brexit.
According to the organizers, “With the clock ticking, stakeholders will consider explicitly in this conference the dimension of time in shaping what opportunities for action companies-and indeed all stakeholders-must consider.”
The closing session, called Brexit time check: "what’s next for medicines?”, will be chaired by ACT columnist Peter O’Donnell. The aim is to investigate the broader level vision of what’s coming next in the Brexit schedule of change.
For the full program and further details, click here.
Philip Ward is the European Editor for Applied Clinical Trials.
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.