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...
The Evolution of Interactive Response Technology (IRT)
Interactive Response Technology (IRT) was initially invented in the 1970s to prevent patient over...
UK clinical trials & participant payments: Experience from across all phases of research
Originally published on the Greenphire website prior to the merger with Suvoda in 2025.
Clinical...
Great IRT Service Makes it Easier for Patients to Participate in Complex Clinical Trials
By: Rob Hummel, Chief Operating Officer, Suvoda