VISTAAR - Global Regulatory Intelligence and Regulatory Information
VISTAAR, global regulatory intelligence specially designed for Regulatory (Strategy, Policy, Operations, Submissions) teams in BioPharma and Medical device companies. It provides updated regulatory data from multiple sources for IRB/clinical submissions, market authorization, safety reporting, manufacturing, LCM and other details.
VISTAAR will keep life science professionals up to date with the constantly changing/evolving regulatory environment with an easy access to continuously updated accurate drug regulatory information.
In addition, custom research projects on regulatory intelligence are also handled by VISTAAR’s experienced team.
What’s included ?
- Ready access to regulatory websites/source of information
- Gives complete control over the entire global drug registration process
- Compare regulatory requirements across countries at a click
- An unequalled depth, breadth of regulatory intelligence, support from a global in-house team of highly qualified regulatory professionals
- Alerts on regulatory changes as an when they happen