Suvoda blog

Clinical trials depend on IRT systems to manage the many variables of patient and drug supply...

By John Ristuccia, Senior Vice President, Global Client Services

Patients living with a rare...

Clinical trials typically encounter delays and disruption. With careful planning and a flexible...

Originally published on the Greenphire website prior to the merger with Suvoda in 2025.

I recently...

Scientists, healthcare leaders and technology leaders have long discussed the potential of an...

Informed consent has been the backbone of ethical clinical trials for the last 70 years. It is...

How IRT Can Streamline Early-Phase Oncology Trials Increasing Control and Agility

By Kelly Snow,...

Successfully conducting a clinical trial to completion is rarely a straightforward and stress-free...

Originally published on the Greenphire website prior to the merger with Suvoda in 2025.

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By Giada Corvino, Services Delivery Manager, Suvoda and Henk Dieteren, Clinical Supply Chain...