Pharmaceutical Market Europe • February 2025 • 20-21
MARKET TRENDS
By Tanya Kogan
One of the most challenging aspects of conducting clinical research is its global nature, as there are significant variances in regional requirements and obstacles. Regulatory, cultural and logistical factors all impact trial design, start-up and execution. Greenphire’s 2024 Market Trends Survey highlights the distinct priorities and hurdles faced by nearly 400 sponsors, contract research organisations (CROs) and sites around the world.
From participant engagement strategies to the role of technology, this report offers valuable insights into the sentiments of the European clinical trial market – and how it compares to the US.
A positive participant experience is crucial for recruitment, retention and trial success. Both regions aim to remove financial and logistical barriers but with emphasis placed on slightly varied areas of support.
Both regions face struggles related to enrolling diverse populations. However, introducing initiatives to increase diversity in clinical trials remains a focus in Europe and the US.
Adopting efficient, patient-, site-centric and GDPR-compliant technology is a shared goal globally but particularly in the EU. Additionally, we see a common sentiment regarding the lack of up-to-date data in support of study cost planning. The survey indicated:
Sites are the backbone of clinical trials worldwide, but operational pressures and administrative burdens remain a challenge no matter the region. Key insights from the survey include:
Operating across Europe requires adaptability, given the region’s diversity and scale. The survey highlights these insights:
Insights from our 2024 Market Trends Survey highlight the current clinical trial landscape, with a unique look into how challenges and priorities differ across two major clinical research markets. From protocol complexity to participant engagement and use of technology, when it comes to conducting clinical trials, the EU and US face similar challenges but with varying nuances and views.
Regardless of the differences, it is clear that there is a shared commitment to driving efficiency and improving support for participants and sites alike. By leveraging this data, sponsors, CROs, sites and solution providers can better direct their efforts and strategies to optimise the areas where there is the greatest need. Ultimately, it is through the voice of these key stakeholders that we as an industry can enhance participant experiences, remove burdens on research sites and improve clinical trial outcomes.
Tanya Kogan is Senior Product Manager at Greenphire