Sponsored Webcast: Beyond Compliance: A Strategic Approach to Clinical Trial Disclosure Maturity (On Demand)
As regulatory scrutiny of clinical trial transparency intensifies, life sciences companies face mounting pressure to evolve their disclosure practices beyond basic compliance. Over 130 new regulatory guidance documents and laws related to clinical trial disclosure were published in the past year alone, with approximately 30% already superseded — highlighting the rapid pace of change.
This session introduces a comprehensive maturity model framework for clinical trial disclosure, helping organizations assess and enhance their capabilities across eight critical domains. By examining real-world scenarios and common challenges, attendees will learn how to evaluate their maturity level and develop a strategic roadmap for improvement. The focus will be practical implementation strategies tailored to different organizational sizes and resource levels, from smaller sponsors managing a few trials to larger organizations with complex global portfolios.
This session introduces a comprehensive maturity model framework for clinical trial disclosure, helping organizations assess and enhance their capabilities across eight critical domains.
Registration Fees & Deadlines
Member: $0 | Nonmember: $50
Learning Objectives
- Understand the three levels of disclosure maturity and how to assess your organization's current state
- Identify critical success factors across key domains, including process management, quality & compliance, and data governance
- Develop a practical roadmap for advancing disclosure maturity based on organizational size and resources
- Implement effective metrics and KPIs to track progress and demonstrate value
Who Should Attend?
- Regulatory affairs professionals
- Clinical trial disclosure managers and teams
- Clinical operations leaders
- Quality assurance personnel
- Medical writers
- Technology and systems managers supporting disclosure
- Clinical development leadership
- Compliance officers
Audience Learning Level
Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.
Speakers
Thomas Wicks
Head of Transparency Operations at TrialScope, Citeline
Thomas Wicks coordinates TrialScope’s operations, consults on the business strategy, and leads the disclosure advisory services. He is responsible for tracking clinical disclosure and data-sharing trends that shape the company’s clinical transparency solutions and services. Thomas has over 25 years of experience with compliance management solutions, specializing in applications for life sciences with a focus on clinical trial disclosure and transparency since 2007.
