Why TrialScope Intelligence?
TrialScope Intelligence is the central solution to better understand and apply clinical trial reporting regulatory requirements. Our in-depth information helps you swiftly leverage your team expertise to plan and prepare trial registrations and results disclosures in compliance with health authorities' requirements, locally and globally.
What information does TrialScope Intelligence provide?
The key information you need is easy to access in one place with our four content pillars:
Health authorities and trial registries detailed requirements – manually curated from the official sources and placed in easy-to-use formats.
Official source documents - PDFs of health authorities and trial registries requirements in their original language and format.
English-language translations – translations of key documents or document sections.
Disclose Perspectives - exclusive articles by experienced journalists and disclosure experts that help you understand the context of regulatory requirements.
How many countries do you cover?
Our coverage is global. We regularly monitor countries without current disclosure requirements to validate their status and detect changes. We will cover about 200 countries. We anticipate there will be 62 countries with known disclosure requirement and/or registries and 134 countries confirmed with no requirements and/or registries.
How many registries do you cover, and do you cover all types of registries?
We cover national or regional registries. Academic and patient registries are not included.