Improving Informed Consent: A Closer Look at the Draft FDA Guidance for Patient Understanding
Author: Amanda Howley, Director, Services Delivery
Snapshot:
- Enhanced Patient Understanding: The...
The benefits of real-time data for CROs
Author: Andrés Escallón, VP eCOA Practice
Snapshot:
Enhanced Decision-Making: Real-time data...
How CROs can meet timelines by selecting fit-for-purpose technology to run their trials
Author: Anthony Encarnacao, Vice President, Global Partnerships
Snapshot: Technological hurdles: ...
Sponsor Checklist: deciding between purpose-built IRT or EDC with IRT add-on
10 questions to help identify an IRT solution
As the complexity of clinical trials continues to...
Two years of AI learning: Looking ahead to what’s coming
Author: Heather Nonnemacher, Associate Director, Services Solutions
Two years of AI learning: Streamlining clinical trials today for future advancements
Author: Heather Nonnemacher, Associate Director, Services Solutions
Improving patient comprehension through eConsent: a win-win for patients, sites, and sponsors
Author: Amanda Howley, Director of Services Delivery
Four steps to forge strong partnerships between CROs, sponsors, and technology vendors
Author: Anthony Encarnacao, Vice President, Global Partnerships
Snapshot: Understanding...
Big ideas for 2024: A conversation with Suvoda CEO Jagath Wanninayake
Author: Elena Filimonova, Chief Marketing Officer
IRT Decision Guidance
A framework to identify the right IRT solution for each trial
With increasing protocol complexity,...