Biopharma
When it comes to regulatory requirements, you need authoritative and up-to-date information that you can rely on; Real time alerts are essential, along with insights on clinical activities in various countries within your therapeutic areas and access to see different product labels for strategic planning purposes.
How Vistaar can help?
At Vistaar, we utilize AI powered technology, in conjunction with our global team of Analysts and SMEs who review and align our broader and deeper datasets to meet your specific needs(in the form of customized reports, targeted searches, timely alerts, and comprehensive monitoring services)
Vistaar Expertise
- Regulatory requirements for Drugs, Biologics, OTC, Generics, Pediatric, and Orphan disease pathways
- Manually reviewed regulatory summaries covering advisory, clinical, IRB, market launches, testing standards, submission checklists, fees, labeling, import/export, marketing, safety/PV, life cycle requirements, and many more areas in a granular manner
- Compare countries or specific areas side-by-side (and download in the format of your preference)
- Search marketed products and their Labels from Canada, US, UK, and EU
- 1.2 Million Global document repository of health authorities’ regulations and guidance, updated daily and provided to you with AI-enabled search for faster and better matches
- 1.4 Million Global document repository of health authorities’ regulations and guidance, updated daily and provided to you with AI-enabled search for faster and better matches
- Global clinical trials gathered from global registries for you to see all clinical activity
- Integrate with any of your existing tools to get this “knowledge” into your daily systems