BIO Convention in San Diego, USA, 23-26 June 2014

June 2, 2014

BIO Convention in San Diego, USA, 23-26 June 2014

Flex Databases will attend BIO Convention in San Diego.

Please contact us at contactus@flexdatabases.com to arrange a prescheduled meeting with Flex Databases!

BIO International Convention is the largest venue for private company-to-company meetings in the world.

Blog

July 21, 2026
Protocol Deviations Start Earlier Than You Think

Most sponsors associate protocol deviations with events that occur later in a clinical trial, like missed visits or incomplete documentation. In reality, one of the earliest and most consequential protocol deviations is happening during patient randomization. Randomization is often perceived as a simple operational step:patient enrolled, button clicked, treatment assigned. But under the pressure of […]

July 17, 2026
Why Long-Established eClinical Platforms Are Slowing Down Modern Clinical Trials 

What Sponsors Should Really Look For When Choosing an eClinical Platform?  Today, every established vendor offers all kinds of system modules, document management capabilities, and a long list of compliance certifications.  On paper, they appear remarkably similar, making it increasingly difficult for sponsors and CROs to distinguish between solutions based on feature lists alone.  In reality, they couldn’t be more different.  Most enterprise eClinical platforms can […]

July 16, 2026
Customize CTMS Dashboards for Every User

Every clinical trial role requires different information. CRAs need to track upcoming monitoring visits, Project Managers need study performance metrics, and clinical operations teams need enrollment and site activity data. In this video, see how Flex Databases CTMS allows every user to create a personalized dashboard without affecting other users. Learn how to add or […]

July 15, 2026
How ITS Cut Manual Safety Tracking by 60% and Strengthened PV Oversight Across Clinical Trials

About Integrated Therapeutic Solutions Integrated Therapeutic Solutions (ITS) is a clinical research organization conducting multi-country clinical trials and supporting post-marketing needs across a growing sponsor portfolio. As case volumes increased, so did the complexity of managing pharmacovigilance activities from safety event intake and workflow tracking to regulatory reporting and cross-functional coordination with clinical operations teams. […]

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