Managing clinical trial disclosure can be challenging with the ever-evolving regulatory landscape, and varying requirements across different jurisdictions and regulatory bodies. New and updated regulations need to be continuously monitored and assessed for potential impact on an organization, processes and overall strategy.
Missing an update can lead to non-compliance and result in severe penalties including fines, sanctions, and reputational damage.
TrialScope Intelligence offers a centralized, interactive repository of critical and accurate insight on global clinical trial disclosure, empowering sponsors of all sizes to efficiently manage disclosure compliance in both development and post-marketing phases.
Countries
Comprehensive regulatory intelligence tracking clinical trial disclosure requirements across nearly every global jurisdiction.Disclosure Requirements
In-depth disclosure requirements covering protocol registration, results disclosure, and contact information, with 59 detailed registry records.International Standards
Comprehensive coverage of major international regulatory frameworks, including WHO, ICMJE, PACTR, and key EU requirements.Source Documents
Extensive library of original regulatory guidelines with English translations, including 130+ new disclosure-related documents annually.TrialScope Intelligence is designed to assist organizations to plan and manage global regulatory developments in a single solution, removing the burden of manually tracking multiple sources of regulatory information.
Streamline complex disclosure demands, enhance process efficiencies, and maintain transparency and public trust.
Access detailed regulatory information in an easily digestible format, reducing manual efforts in monitoring and curating requirements.
Minimize the time spent gathering and interpreting global disclosure requirements with extensive coverage.
How it works
Our experts monitor, collect, and curate regulatory intelligence and insight. Disclose Perspectives articles are crafted by experienced journalists specializing in biopharma policy and business information, offering a tailored solution for clinical trial disclosure and regulatory intelligence professionals.
Comprehensive coverage of regulatory authority and trial registry requirements for over 195+ countries.
Review global health authority and trial registry regulations in their original language, context, and format.
Access translated versions of crucial disclosure documents and passages using human insight.
Exclusive insights and trends on the latest disclosure developments from experts and journalists.
Annotate requirements, leave notes and questions for colleagues, and ensure smooth collaboration.
Consult with experts for additional insights on regulatory interpretation and intricacies.
Contact us today to learn how we can support your clinical trial disclosure needs with critical regulatory and compliance insight.