clinical trial solution

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www.clinion.com

• Clinical Trial Solutions

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About Clinion

• Clinion provides a fully featured, 21 CFR part 11
  compliant EDC solution, giving both investigators
  and monitors a powerful yet easy-to-use
  environment for data entry and monitoring.

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Why Clinion

• You can rapidly transform complex protocols into
  a production-ready EDC study, saving time and
  resources.
• Powerful edit check and testing capabilities
  enabling collaborative development.
• A design environment with secure roles and rights
  that allows multiple users to work on a single
  study without affecting each others changes,
  increasing speed and productivity.
• Templates and a rule development wizard that
  enable non-programmers to quickly and easily
  develop complex rules and edit checks so you save
  time and move your study to production more
  quickly.

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• Rich and robust library functionality that
  facilitates sophisticated search and reuse of
  existing study design assets so you accelerate
  development time and ensure adherence to company
  standards.
• Detailed audit history reports that let you track
  changes on any study or library object so you can
  easily understand who did what and when,
  increasing transparency and minimizing risk.
• Built-in query workflow management permits quick
  DCF resolution so you can easily keep study on
  track.

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Our Vision

• The search for perfection is an integral part of
  our corporate culture. We will be a leading data
  management solution provider by delivering
  compelling value propositions to the global
  healthcare industry. We put all our efforts,
  skill, expertise and dedication into developing a
  solution that perfectly meets your needs.

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Our Mission

• To reduce project risk and cost to Sponsor and to
  expedite the Clinical Trial Process with
  ClinionTM EDC solutions
• Reduce project risk and improve quality with
  ClinionTM EDC solutions.
• Lower total cost of ownership with complete
  ClinionTM EDC solutions.
• Realize faster time to business value by
  leveraging ClinionTM by help of unique library of
  consulting assets and accelerators.

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Clinion Features

• Electronic Data Capture (EDC)
• Clinical Data Management (CDM)
• Common Modules

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Electronic Data Capture (EDC)

• The EDC modules of Clinion are focused on
  simplifying workflows and increasing usability.
  The electronic CRF wholly resembles its paper
  counterpart for easy data capture and seamless
  data integration. The intuitive and user-friendly
  data capture features enable users to interact
  with the system in a way that is most familiar to
  the user.

TM
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Clinical Data Management (CDM)

• Many clinical trials continue to utilize
  paper-driven processes, even as sponsors and
  sites advance toward EDC adoption. Using Clinion,
  data from papers can be effortlessly and
  seamlessly captured into the CDM system.
• Data from case report forms, which are manually
  filled at site, can be transferred to the Clinion
  CDM through data entry. To reduce the possibility
  of errors due to human entry, the systems employ
  various validation checks to verify the data.

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Common Modules

• These are the common modules we have in Clinion
• Study configuration
• Data extraction
• Medical Coding
• Data security integrity
• Database Lock
• Data Loading
• Data Validation
• Study Documents
• Conditional Branching
• Global Libraries
• Profile Set-Up

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Our Clients

• Clinion has been implemented by leading pharma
  companies and CROs, across the world, for a
  variety of clinical trial processes. Some of our
  clients and partners include

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Contact Us

• Please write to us at info_at_quadone.com
• CORPORATE OFFICE
• 728, Venkateswara Hills,
• Opp Times of India,
• Road No 3, Banjara Hills
• Hyderabad 500034
• INDIA

Phones INDIA 91 40 2335 0221 91 40 2335 0321
(Telefax)
US 1 201 484 7621 1 646 202 1452