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clinical trial solution

clinical trial solution

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clinical trial solution

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  1. Clinical Trial Solutions

  2. 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.

  3. 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 other’s 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.

  4. 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.

  5. 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.

  6. 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.

  7. Clinion Features • Electronic Data Capture (EDC) • Clinical Data Management (CDM) • Common Modules

  8. Electronic Data Capture (EDC) TM 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.

  9. 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.

  10. 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

  11. 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:

  12. Contact Us Please write to us 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