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7 responsibilities for life science service providers to ensure ICH-GCP compliance
For life science service or technology providers engaged in clinical research, it’s imperative to ensure compliance with international standards. Even though the ultimate responsibility for compliance lies with…
Patient engagement in clinical trials: Why it matters and how to improve it
Recruiting patients for clinical trials is only half of the battle. Retaining those eligible patients over the course of the study to ensure reliable data is another…
Clinical Trial Technology: Why IT Infrastructure & Security Matters
From internal communication and management systems to tools sponsors deploy to improve operations and results, technology is everywhere in the clinical trial landscape. However, these technologies are…
Clinical Trial Technology & Project Management:
4 Aspects of Cognivia’s Approach
Many sponsors err on the side of reluctance when incorporating new technology in clinical trials. This is because some technologies have the potential to overly burden not…
Q&A: Experts’ Perspectives on the Placebo Response in Clinical Trials
Experts shared their perspectives from real-world trials on both classical and new approaches to manage the placebo response – and some questions arose throughout the discussion.
Q&A: Developing a Custom e-Questionnaire Data Management Solution for Clinical Trials
Q&A Interview with Gilles Scuttenaire, Senior Software Engineer In a presentation at BIO IT World 2022, Cognivia’s Gilles Scuttenaire, senior Software Engineer, discussed our custom, end-to-end data management…
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