No More Swiss Holes: Filling the Gaps in Clinical Trial Disclosure
Use Case
Regulatory & Compliance
TrialScope Intelligence — a centralized, interactive repository of global clinical trial disclosure regulations and insights — maintains 193 country records, 59 registry records, and over 1,000 authoritative regulatory texts globally.
Download
FAQ
Is clinical trial registration mandatory in Switzerland?
Yes. Under Swiss law, clinical trial registration is legally required for interventional studies. Sponsors must register the trial before it starts and within six months after approval has been granted.
Which registries must be used for trial registration in Switzerland?
Switzerland requires dual registration: one in a WHO Primary Registry (such as ClinicalTrials.gov) and one in the local Swiss registry, Human Research Switzerland (HumRes).
What details does TrialScope Intelligence include?
TrialScope Intelligence’s registry records include official registry names, URLs, account creation steps, technical support contacts, and detailed field mappings for required data. These records outline submission workflows, validation checks, amendment processes, and timelines for public posting.
Related products
TrialScope Intelligence
A centralized, interactive repository of the critical regulatory knowledge needed for global clinical trial disclosure compliance
TrialScope Disclose
Manage the complexity of clinical trial disclosure and the risk of noncompliance by automating data entry and reporting to registries
Trial Summaries
This user-friendly portal aggregates clinical trial results summaries across sponsors
SEP 15, 2025
Webinar
Regulatory & Compliance
Global Clinical Trial Disclosure Fundamentals — Requirements, Timing, and Enforcement Consequences
Catch up on core disclosure requirements: what must be disclosed, when, and how. Learn about enforcement mechanisms and why maintaining compliance is crucial.
