assisTek’s Direct Clinical Data Capture (DCDC) module was designed to eliminate paper documents used to record source data in clinical trials. The system can be used to capture a range of data, such as Vital Signs, Adverse Events, and Investigational Product Verification. All fields and features can be customized to fit any clinical trial protocol requirement.
The DCDC module features the use of a 10” Tablet which is large enough to easily work from, but highly portable for use in any busy medical office or home setting. All patient data recorded in the DCDC system will be available immediately to all study team members for review and follow-up because the system automatically transmits data at all times using a cellular network.
The DCDC module can be utilized by various users including: Study Coordinators/Nurses, Patients, and Investigators. The versatility of this module makes it a truly unique solution.
According to the FDA guidance on source data in electronic form, eSource will help to eliminate unnecessary duplication of data, reduce the opportunity for transcription errors, promote the real-time entry of electronic source data during subject visits, ensure the accuracy and completeness of data, and more.
|assisTek's TotalSource solutions capture these improvements to source data, and are customized to each individual protocol.||More Information|
assisTek successfully fuses new developments in mobile technology with creative software solutions to revolutionize the collection of data from patients and clinicians in clinical trials. We have proudly been helping clinical trial teams achieve success for over 18 years, in 40 countries with 46 languages. Our expertise can support studies in any phase.More Information