Better Clinical Trials
The clinical research industry is responsible for the delivery of novel medical solutions to society. Its core purpose is the systematic evaluation of candidate medical solutions in clinical trials. It often takes 10-12 years of highly regulated clinical trials to bring a single medical solution to the patient.
Each clinical trial involves a number of specialty stakeholders spanning various organizations and societal domains. Throughout a trial, these stakeholders need to interact in a broad range of trial-related activities, ranging from study approval to site monitoring, regulatory filing and research dissemination.
Complex and Resource-inefficient
Unfortunately, the clinical research industry is characterized by a number of issues that make the innovation process overly complex, lengthy and resource-inefficient.
- Lack of oversight
- Difficulty in record keeping
- Reduced trust and impaired reputation
- Low patient engagement
Together with Triall.io we bring together a consortium of clinical trial specialists and blockchain engineers to tackle some of the persisting issues that make clinical trial operations overly complex, lengthy, and resource-inefficient.
Verial, a clinical document management solution
Verial is a first, a clinical document management solution that enables users to establish verifiable proof of the integrity and authenticity of essential research documents, and to establish an immutable audit trail of their evolution over the course of a clinical trial.
Verial generates proof that these documents have not been altered after registration. It drastically improves the reliability and auditability of clinical research throughout the pharmaceutical development chain, and fully answers to calls for meticulous documentation and data transparency by the U.S. Food & Drug Administration (FDA), European Medicine Agency (EMA), and other regulatory authorities.