Intel and Insights
GOTO Place for Pharma, Biotech and Medical Device companies
VISTAAR is most up-to-date compared to any other Intel or data source because we use smart artificial intelligence methods all through out. With a unique combination of technology and smart people, you will get your strategy and trusted insights much faster. Over many years, VISTAAR has built deep data sets to help you on your Regulatory and Clinical projects. All this done at the best price point in the industry.
Save your time with ready made country specific regulatory requirements report for 112 Countries
Global clinical trial data with country specific registries for better search flexibility and deeper research by employing artificial intelligence under real-life conditions
Assisting teams to make right decisions for product development, maintenance and Regulatory compliance with real-time Intelligence
1.2M documents from several Health Authorities & related govt agencies
You give your thoughts / plans in few simple answers and VISTAAR provides some ADVISORY scenarios for you. Different playbooks included to get you started.
VISTAAR Insights
Consultation on GMP and Compounded Medicines...
The Therapeutic Goods Administration’s (TGA)...
Classification for Medical Devices and IVDs -...
Indian regulatory authority for healthcare, CDSCO...
Medical Device Surveillance System in Spain
The prime objective of the Health Products...
ANSM’s Enhanced Pharmacovigilance Service in...
ANSM has established a monitoring system specific...