Clinical Trials

The extensive process behind producing a safe, effective drug or product is expensive. Yet, life sciences companies are under increased pressure to build a robust pipeline, while reducing research and development costs. Among the key challenges facing sponsors, investigators, partners, and clinical research organizations (CROs) is how to manage the large volume of electronic and paper documents and forms more efficiently, cost-effectively, and securely. According to statistics published by PhRMA, life sciences companies spend approximately 40% of their R&D budgets managing manual, paper-based processes.

Research and Development (R&D) departments develop new products and services that can create competitive advantage in the marketplace. Success depends on developing superior, protected, proprietary products and services. R&D staff such as scientists, engineers and technicians have unique perspectives, which necessitate agile and efficient data capture processes to support research and knowledge exchange with colleagues, customers, partners and suppliers.

Dataintro helps life sciences companies streamline clinical trials processes by:

  • Reducing time to market: Improve the clinical trials process and shorten product development cycles with automated, intelligent forms.
  • Tracking interactions efficiently: Provide an auditable form process history to streamline compliance requirements.
  • Decreasing the costs and risks of distributing confidential information: Apply persistent and dynamic security policies to control how, when, and by whom documents can be accessed.
  • Reducing research costs: Use free PDF reader software to quickly collect information and help shorten the costly development cycle.

Dataintro solutions for Research and Development departments recognize that R&D information is particularly diverse and must be maintained for proprietary advantage.

Our solutions will help you to:

  • Reduce cycle time by automating processes
  • Respond more rapidly to regulatory requests and updates
  • Allow investigators to electronically access and complete PDF forms from clinical trial web portals for printing and mailing.
  • Require no additional hardware/software investment than a free PDF Reader
  • Provide anytime, anywhere access to forms for completion online or offline using a free PDF reader.
  • Enable automated, real-time data capture, which reduces costs, errors, and time compared with manual data entry.

Use Dataintro Clinical Trial solutions to automate the capture of fill-and-print paper form data; 2D barcode on the form encodes end user data, and the company simply scans the 2D barcode to extract and pass the data into its core systems