Global Regulatory and Clinical Intelligence Software - VISTAAR - PowerPoint PPT Presentation

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Global Regulatory and Clinical Intelligence Software - VISTAAR

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VISTAAR combines regulatory content compiled by experts with advanced technology (AI) to deliver a unique regulatory intelligence solution addressing the regulatory landscape including Classification, Clinical, Marketing, Labeling, Safety, Variations, Imports/Exports and other key areas based on the inbuilt proprietary algorithms that align with regulatory and clinical business goals. – PowerPoint PPT presentation

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Title: Global Regulatory and Clinical Intelligence Software - VISTAAR


1
Global Regulatory and Clinical Intelligence
Platform
www. v i st a a r . a i
2
DDi Announces VISTAAR to redefine Regulatory
Intelligence with
AI enabled Technology
Leveraging Artificial Intelligence, technology
provides comprehensive coverage and actionable
insights on global regulatory information for
drugs, biologics, and devices of about 90
countries.
WWW.VISTAAR.AI
3
Keeping compliant with the ever-changing global
regulatory environment and quality standards is
key to professionals involved in manufacturing,
launching, and post-marketing surveillance of
drugs and medical devices. The growth in the
number and complexity of regulations and quality
standards is posing several challenges to
companies. Traditional Regulatory intelligence
(RI) systems are not keeping with changing times
and adapting technology to get Regulatory
Affairs teams right Insights at higher Return
on Investment (ROI). With a variety of
information sources, identifying and analyzing
what you need for submissions is a time-consuming
task. To make correct decisions for your
organization, easy and speed access to correct
information makes all the difference. VISTAAR is
a Global Regulatory and Clinical Intelligence
Platform which focuses exclusively on providing
Regulatory Intelligence(RI) and Clinical
Intelligence (Clin Intel) solution for drugs,
devices, combination products, biologics,
generics, active pharmaceutical ingredients and
animal health drugs thereby supporting
pharmaceutical and medical device companies
starting from overview of any countrys
regulations or requirement to assess the
regulatory needs for product registration and
answering to any focused regulatory query.
WWW.VISTAAR.AI
4
SUMMARIZE
Pre-compiled regulatory summaries for drugs,
devices, combination products, biologics,
generics, active pharmaceutical ingredients and
animal health drugs of about 90 countries
compiled by experts and updated frequently.
IT' S CORE FEATURES INCLUDE
HUNT It uses artificial intelligence (NLP,
machine learning) to get you right documents for
your queries/needs.
REG BOT
With its chat interface gets you information
faster for your simpler questions by using AI
techniques at the backend.
5
MARKET PLACE
With It's Unique NO involvement policy VISTAARs
Market Place helps companies find the right
consultants for their needs and Independent
Consultants to meet Companies who need their
Services.
IT' S CORE FEATURES INCLUDE
STANDARDS Keep you informed about the medical
device quality standards updates and about which
product is affected by the changes through
e-mail notifications. MY COLLECTIONS Lets you
store and share links, documents, and more.
6
ANALYZE
(Coming up in May 2019) Document Analyzer
assists the user to analyze the scope of the
specific document, analyzes the content and
displays the summary and scope of the
information.
IT' S CORE FEATURES INCLUDE
CLIN INTEL (coming up in June 2019)
7
USE VISTAARS INTELLIGENCE TO
  • Access continuously updated regulatory
    intelligence requirements and quality standards
  • Reduce the complexity of Regulatory and Clinical
    teams going through the sheer volume of
    regulatory documents (and a lot of them are
    irrelevant) by providing summarized regulatory
    content based on your organization needs.
  • Be cost-effective with an easy-to-use interface,
    and a comprehensive collection of regulatory
    content. Understand submission routes and local
    regulatory practices
  • Compare regulatory requirements across countries
  • Provides updated regulatory data from multiple
    sources, both authoritative (health agencies) and
    other channels
  • Increases RA productivity drastically
  • Decrease your Regulatory Intelligence costs by at
    least 50
  • Maintains the centralized repository for
    regulatory intelligence or policy documents
  • Monitors and tracks all Status changes,
    amendments or additional medical device quality
    standard initiatives.
  • WWW.VISTAAR.AI

8
VISTAAR combines regulatory content compiled by
experts with advanced technology (AI) to deliver
a unique regulatory intelligence solution
addressing the regulatory landscape including
Classification, Clinical, Marketing, Labeling,
Safety, Variations, Imports/Exports and other
key areas based on the inbuilt proprietary
algorithms that align with regulatory and
clinical business goals.
Visit us www.vistaar.ai
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