DIA 2023: key takeaways of the event

July 13, 2023

DIA 2023: key takeaways of the event

As always, DIA 2023 was mostly about the people we meet & talk to, but there is a big second value to it – the talks, the ideas and insights that we get during the conference. Let’s take a look at what’s hot in Boston!

  • Embracing Technology: The conference highlighted the use of technology in clinical trials. Agile methodologies, which were originally used in software development, are now being recognized and adopted in the life sciences field. These methods are seen as beneficial for managing the complex demands of clinical trials. Digital health technologies were also emphasized for improving efficiency, patient engagement, and overall trial success.
  • Addressing Regulatory Challenges: A significant portion of the conference focused on regulatory challenges and strategies to ensure future-proof processes. The importance of aligning regulatory timelines and submissions was emphasized. Discussions also revolved around pharmacovigilance, including regulatory views on post-pandemic inspections and risk-minimization measures.
  • Advancements in Data Management: The conference explored the role of artificial intelligence (AI) and large language models in clinical trials. These technologies can help identify biomarkers and improve efficiency in clinical research. AI was discussed as a means to expedite data collection and analysis, thereby streamlining trial procedures. The significance of a modern clinical data ecosystem equipped with embedded AI was highlighted.
  • Patient-Centric Approach: The conference emphasized the crucial role of patients in drug development and clinical trials. Evaluating the impact of patient involvement across research and development (R&D) was emphasized. Patient-led approaches in clinical trial design and execution were explored. The importance of patient engagement and public-private partnerships in drug development was also discussed.

We can’t wait to be back in 2024!

Blog

July 22, 2025
Electronic Data Capture – Everything You Need To Know

What is Electronic Data Capture? Electronic Data Capture (EDC) is an electronic system applied to clinical trials for capturing, managing, and storing patient data. Instead of paper-based forms, investigators enter clinical trial information directly into a secure, web-based site. EDC systems validate data integrity, reduce errors, and automate the data collection process – accelerating clinical […]

Data Hosting with Confidence – Flex SaaS for Clinical Trial Environments 

At Flex Databases, we deliver a SaaS solution purpose-built for clinical trials – offering global accessibility with full transparency and control over where your data resides.  Not a Public Cloud. A Dedicated SaaS Platform You Can Trust.  Flex Databases is an EU-based company operating globally and trusted by life sciences organizations for secure, validated SaaS […]

July 14, 2025
What is CTMS? Frequently Asked Questions

What is CTMS A CTMS – Clinical Trial Management System is a software solution that facilitates more streamlined management and monitoring of clinical trials. Clinical operations teams like project managers, CRAs, and study coordinators in pharmaceutical firms, CROs, and biotech firms use the tool to oversee everything from site selection and subject recruitment to monitoring […]

July 3, 2025
Everest CRO Experience with Flex Databases

Dana Leff Niedzielska, MBA, SVP of Global Clinical Operations at Everest Clinical Research, shares her experience using Flex Databases’ CTMS and eTMF. In this interview, Dana highlights how Flex Databases supports Everest CRO’s clinical operations. Learn why Everest chose Flex Databases as their trusted technology partner and why they continue to rely on and trust […]

Contact us

Get in touch to discuss compliance, implementation, demos, pricing

We are here for all of your questions! Tell us more about yourself and we will organize a tailored live demo to show how you can power up your clinical trials processes with Flex Databases.