3 ways flexible technology supports the complexity of rare disease trials
By John Ristuccia, Senior Vice President, Global Client Services
Patients living with a rare...
Closing the gap between trial plan and reality
Clinical trials typically encounter delays and disruption. With careful planning and a flexible...
Trust, awareness and access: The three keys to sustaining diversity in clinical trials
Originally published on the Greenphire website prior to the merger with Suvoda in 2025.
I recently...
eConsent Across Multiple Geographies and Regulations
Scientists, healthcare leaders and technology leaders have long discussed the potential of an...
eConsent + IRT: Elegant consent management for all
Informed consent has been the backbone of ethical clinical trials for the last 70 years. It is...
Flexible IRT for early-phase oncology trials
How IRT Can Streamline Early-Phase Oncology Trials Increasing Control and Agility
By Kelly Snow,...
Why clinical trials need expert support for ongoing success
Successfully conducting a clinical trial to completion is rarely a straightforward and stress-free...
Leveraging data for efficient and intelligent budget creation and negotiation
Originally published on the Greenphire website prior to the merger with Suvoda in 2025.
...
Top 5 logistical considerations for global clinical studies
By Giada Corvino, Services Delivery Manager, Suvoda and Henk Dieteren, Clinical Supply Chain...
10 Crucial IRT Features that Deserve a Nuanced Approach
Interactive Response Technology (IRT) plays a vital role within the eClinical technology ecosystem...