Stay ahead of a complex and constantly evolving disclosure landscape.
Access regulatory authority and trial registry requirements across 195+ jurisdictions.
Centralize complex disclosure obligations and support consistent interpretation across teams.
Reduce time spent gathering, translating, and assessing global disclosure requirements.
Identify relevant updates earlier to help reduce noncompliance risk, penalties, and reputational exposure.
Review country, registry, and requirement records supported by source documents for protocol registration, results posting, plain-language summaries, enforcement, and more.
Assess and review disclosure requirements across multiple countries broken down into protocol and results details, based on study type and phase.
Review original regulations in their native language, context, and format for deeper analysis and audit support.
Comprehensive monitoring of regulatory authority and registry requirements worldwide, so no obligation goes untracked.
Use expert analysis and Intelligence Perspectives articles to anticipate clinical trial disclosure and transparency developments.
Add private notes and comments to improve cross-functional alignment and knowledge sharing across your organization.
Set up alerts on requirement and registry records relevant to your portfolio and choose how often you are notified.
Engage subject matter experts directly for additional insight into regulatory interpretation and disclosure intricacies.
Identify relevant updates earlier to reduce noncompliance risk, regulatory penalties, and reputational exposure.
Use expert analysis and Intelligence Perspectives to anticipate clinical trial disclosure and transparency developments before they affect your compliance strategy.
Access source regulations in their original language, context, and format for deeper review and audit support — backed by human-reviewed translations for selected documents.
Add private notes and comments to requirement and registry records to improve cross-functional alignment and build a shared knowledge base across regulatory, legal, and clinical teams.
Engage Citeline’s subject matter experts directly for additional insight into regulatory interpretation, jurisdictional nuances, and complex disclosure intricacies.
Speak to a Citeline expert to discuss your use case, access needs, and the right setup for your organization.
TrialScope Intelligence is a centralized regulatory intelligence platform that tracks clinical trial disclosure requirements across 195+ global jurisdictions, helping sponsors monitor, interpret, and act on their disclosure obligations.
It covers protocol registration, results posting, plain-language summaries, enforcement provisions, and more — including whether obligations are mandatory, voluntary, or not defined across each jurisdiction.
All requirements are grounded in 1,300+ primary source documents captured directly from official health authorities and legislation — not secondary interpretation.
Citeline’s regulatory experts continuously monitor global health authorities and trial registries, ensuring that requirement records and Intelligence Perspectives articles reflect the latest regulatory changes.
Yes. TrialScope Intelligence lets you assess and compare disclosure requirements across multiple countries, broken down by protocol and results details and filtered by study type and phase.
Yes. You can access source regulations in their original language alongside human-reviewed English translations for selected key disclosure documents.
Yes. TrialScope Intelligence allows you to create alerts on specific requirement and registry records and choose the frequency of notifications to stay informed on changes that matter most to your team.
Regulatory affairs, clinical trial transparency, legal, and compliance teams at pharmaceutical sponsors who need to manage and monitor global disclosure obligations efficiently.
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