How IRT flexibility supports rare disease trials
By Miranda Blanchard and Shery Pfeifer, Suvoda Senior Design Consultants, Design Leads
The Building Blocks of IRT Customer Satisfaction
Clinical trials depend on IRT systems to manage the many variables of patient and drug supply...
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...
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...
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...