TrialScope Intelligence: Critical Insight For Global Clinical Trial Disclosure Compliance
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 noncompliance 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.
TrialScope Intelligence by the numbers
195+ Countries
Comprehensive regulatory intelligence tracking clinical trial disclosure requirements across nearly every global jurisdiction.
75+ Disclosure Requirements
In-depth disclosure requirements covering protocol registration, results disclosure, and contact information, with 59 detailed registry records.
10 International Standards
Comprehensive coverage of major international regulatory frameworks, including WHO, ICMJE, PACTR, and key EU requirements.
900+ Source Documents
Extensive library of original regulatory guidelines with English translations, including 130+ new disclosure-related documents annually.
How it helps
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.
Simplified Management
Streamline complex disclosure demands, enhance process efficiencies, and maintain transparency and public trust.
Comprehensive Coverage
Access detailed regulatory information in an easily digestible format, reducing manual efforts in monitoring and curating requirements.
Time Efficiency
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.
What's included
Regulatory Requirements
Comprehensive coverage of regulatory authority and trial registry requirements for over 195+ countries.
Original Regulations
Review global health authority and trial registry regulations in their original language, context, and format.
Translations
Access translated versions of crucial disclosure documents and passages using human insight.
Expert Analysis
Exclusive insights and trends on the latest disclosure developments from experts and journalists.
Collaboration Tools
Annotate requirements, leave notes and questions for colleagues, and ensure smooth collaboration.
Ask the Analyst
Consult with experts for additional insights on regulatory interpretation and intricacies.
Our experts
When it comes to the drug development process, regulatory is one area that simply cannot be overlooked; too much is at stake. Citeline’s regulatory intelligence, solutions and services help ensure that your organization maintains compliance.
The industry’s leading experts on clinical trial disclosure inform our TrialScope Disclose and TrialScope Intelligence Solutions as well as our Disclosure Services.