An up to date collection of regulatory summary reports of about 100+ countries. Compiled by experts and updated frequently; these are a big time saver for you. Information included for drugs, biologics, and medical devices. Some of the data elements include clinical trials, market authorization/registration, import/export, variations/changes, labeling, safety and other key areas.
We can relate to your hours and hours of time spent on search engines or health agencies websites to get right regulations or guidance documents. Either some countries have too much information or for some countries it’s tough to get to right website folders. Our database has 980K documents and are updated on daily basis (using automation) so that you don’t miss any. VISTAAR uses artificial intelligence (NLP, machine learning) to get you right documents for your queries / needs. Enter a question or keyword set to get your full documents, faster. Save your time on searching and rather use that on analyzing or your strategizing.
Vistaar SUMMARIZE and HUNT can help users when they know what exactly they want. Lot of users when going into new markets, or planning to change their product elements and want to know the impact on introducing new product or to support their R&D teams, have ideas and thoughts but may not have a question clearly framed. Vistaar while driving initial probing questions, you can give your needs or plans in simple English. Vistaar by leveraging its AI engine provides you a Regulatory strategy on what is needed, options, country requirements, forms/checklists, what other companies are doing in that scenario, what other products have those situations or parameters and more. Advisory Playbooks acts as your guide or use to verify or as 2nd opinion of your initial plans.
Product Intel is an Insights module that allows user to compare and contrast across products. It provides side-by-side comparisons of indications, side effects, warnings, interactions and more. This module of VISTAAR provides a standard, comprehensive, up-to-date, lookup and download options for marketed drugs and devices.
Global clinical trials and product pipelines by company, by therapeutic area, by indications, by region to form your product specific strategies.
Keeping up to date with required standards is key for medical devices to be compliant in different countries. As Standards are developed by several agencies / bodies, keeping track of who’s updating what is a very manual task. VISTAAR standards module keeps you current on the Standards on who’s updating what and the current versions with other details.
RegBot with it’s chat interface gets you information faster for your simpler questions. “Always on”, this chat application saves you time in searching and gets simpler answers faster by using AI techniques at backend.
Though you are a specialist, there will always be those questions that you don't have an answer or need second opinion. A whole community exists out there. If you are a company, VISTAAR's Market Place lets you find experts/consultants by posting your projects or questions. If you are an independent professional, this is an opportunity to make that extra cash, on full time or part time basis. VISTAAR's role is only initial match making and let's you deal next steps at your will and terms.
If you are working for a large company and ever tried asking for a special/separate Intel repository for you and your teams to organize documents or reports that you create? Chances are high you may have been given what your company use already (like Share point or Documentum) and for you that is a compromise. If you are an individual or working for a small company, your current repository may be either a shared folder or a desktop. Not be an efficient way.
"My Collection" let's you store and share links, documents, and more. Share through LinkedIn or Gmail both internally (in your company) or externally to other members. You will be in control!