VISTAAR

VISTAAR provides Global Regulatory, Clinical, and Compliance Requirements to BioPhrama, Devices, Consumer Health, Cosmetics, and Digital Health. With a unique combination of smart technology and subject experts, you will get up-to-date requirements and trusted insights accurately and much faster. Over many years, VISTAAR has built deep data sets to help you do the right strategy. All this is done at the best price point in the industry. Functionality & Modules: Summarize - Regulatory Requirements database & reports HUNT (includes alerts, watchlist, workflow, sharing, documents/forms creation and full workflow process along with project management tracking) Hunt - Health Authority Documents Repository...

Medical devices regulations,clinical trial regulations,medical devices regulations eu,medical devices regulations canada,fda cosmetics regulations,regulatory intelligence,clinical trials database,medical device labeling requirements,medical device labels,cosmetics labeling requirements,medical device labeling,fda labeling requirements,pharmaceutical and biotech intelligence,medical device regulatory intelligence,drug regulatory intelligence,product intelligence,clinical trial intelligence,regulatory compliance,clinical trial compliance,regulatory updates,regulatory guidelines,new regulations,regulation changes,product comparisons,regulatory strategy,diagnostics regulatory requirements database,consumer healthcare,cosmetics,and drug and device labels

Vistaar operates in the Software development industry.

Vistaar's revenue is 11m - 100m

Vistaar has 11 - 50 employees.