VISTAAR
Software DevelopmentNew Jersey, United States51-200 Employees
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 (1.5 Million) Clin Intel - Global Clinical Trials repository Label Intel - Marketed product labels (USA, EU, Canada & UK) Labels Compliance