Do you find collecting and mining information a challenge?
TrialScope Intelligence empowers sponsors of all sizes to manage clinical trial disclosures efficiently and reduce the risk of non-compliance. It is comprehensive and centralizes all the regulatory knowledge you need in a user friendly format.
Simplify the management of increasingly complex clinical trial disclosure demands. Build efficiencies into your processes and increase your transparency while preserving public trust. Use a robust solution and take the manual strain out of monitoring, collecting, and curating regulatory requirements.
Using TrialScope Intelligence reduces manual work, leaving your team more time to strategize and plan out timely, high-quality, and compliant clinical trial disclosures – in the countries that are relevant to you.
TrialScope Intelligence all-in-one solution provides you with:
- Granular, country specific clinical trial disclosure requirements
- English translations of disclosure requirements
- Collaborative, centralized communication across your organization
- Alerts to new or changing requirements
- Disclosure perspectives, analysis and strategic insights
- Professional support from the included Ask-the-Analyst® service
How it Helps
Dramatically reduce the time you spend gathering and interpreting disclosure requirements
Support your decision making with insights from journalists and Ask-the-Analyst® subject matter experts
Capture your thoughts in context, collaborate with colleagues and favor alignment with external partners