Product Overview
Secure, flexible, and convenient data capture
eCaseLink eConsent can be used as a standalone or part of the fully harmonized unified eCaseLink EDC platform. It captures participant data conveniently on-site or off-site using any web-connected devices such as smartphones, iPads, mini tablets, laptops and desktops. The eConsent system provides all users a secure responsive patient-centric design. This design enables participants to view study-related documentation and grant esignature consent to take part in a clinical trial. It saves valuable time at study sites.
Flexible and convenient data capture
eCaseLink eConsent is a simple intuitive tool designed for real-time, real-site, anywhere data collection situations. This includes operating rooms, clinics, doctor’s offices, or fully remote locations. The application ensures that participant consent time/date and signature is accurately recorded, and investigator signature is also recorded. This eliminates the potential of review findings.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Multimedia information
eCaseLink eConsent provides study information to potential study participants. This includes written, visual, and audio-visual formats. These formats enable optimal information exchange.
- More efficient and effective for participant understanding of content
- Presents information in multi-media fashion and not linear on paper is more effective
- Real-time data collection and TeleHealth support
- Built in eSignature functionality
- Promotes remote monitoring, improving data quality and participant engagement
- Supports interactive videos and other validated assessment tools
About the company
With over 30 years of eClinical experience our roots run deep within the clinical trial study and life sciences industries. Since our founding in 1992, DSG has produced the most innovative software solutions for the pharmaceutical, medical device and life sciences industries world-wide.
DSG’s clinical trial software and data management services have grown over the years because of our understanding of new technologies and our collaborative approach with our clients. In our beginning, and before the internet became mainstream, DSG pioneered CRF document management software, setting an industry standard. Our best-of-breed eCaseLink allowed individuals to build CRFs electronically, greatly reducing the amount of time it takes to run a clinical trial. eCaseLink became the industry standard, and has been trusted and utilized world-wide by the top 5 pharmaceutical companies since 1992.
