Thomas Wicks
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Latest From Thomas Wicks
Robust Trial Transparency Strategy Boosts Patient Engagement
Most clinical trial sponsors view data disclosure as a mandate, maintaining regulatory compliance as a legal requirement. Study sponsors that realize the potential to repurpose this data, using a patient-first approach, turn transparency into a strategic advantage for engagement and recruitment efforts.
5 Steps To Mastering Global Clinical Trial Disclosure Compliance
Clinical trial disclosure compliance must include identification and documentation of registry requirements, key stakeholders, company policies, systems, and processes.
Clinical Data Transparency Is Big Challenge For Smaller Sponsors
Robust transparency, and perhaps even just compliance with evolving requirements of multiple regulators, requires commitment from the C-suite for companies of all sizes.
The Hidden Implications of Clinical Trial Disclosure Noncompliance
Potential fallout from noncompliance goes well beyond regulatory penalties; adherence has improved but less so for smaller companies.