With smart and automated real-time data validation we efficiently reduce up to 80 % of manual data cleaning efforts. Patient data is easy monitorable in modern and lucid interfaces for power users like CRAs, data- or project managers. Role-based access control and audit trails grant full transparency.
- Real-time data validation
- Easy monitorable data
Smart picker for fast selection and accurate coding of adverse events, medical histories, and medications using MedD0RA, WHO-DD, NCI, ICD, OPS, ICD-O-3 m / t.
Automated randomization of patients upon registry.
Standardized tumor assessment according to RECIST-Criteria.
Patient Reported Outcomes
Over 40 readily available standard patient questionnaires and surveys for electronic use.
An electronic medication diary that helps patients to keep up with their oral medication intake and easily complete documentation.
Freetext entries can be directly translated in the eCRF.
The Alcedis Framework supports a range of languages like English, French, Spanish, Italian, Chinese, Russian and much more.
User adaptive dashboard instruments are providing valuable oversight informations. Status of site activities, patient recruitment, completeness of documentation, reached milestones and much more can be individually bookmarked or dynamically found via semantic, elastic search. Forecasting systems and alerts secure that the study is on track.
- In-App Bookmarking to keep the most relevant information always in sight
- Elastic search to find answers to important questions quickly
Confidently manage pharmacovigilance processes with maximum safety and in compliance with regulations.
Transparent, compliant and secure remuneration and payment processing of investigators or study participants.
Be organized at any time. Schedule patient or Monitor appointments at a site, create visit planer and work with a smart reminder and alert functionalities that will assure not to miss an event in your calender.
Streamline the process of site interaction in creating and handling queries. Keep oversight of data cleaning activities and open to-dos.
Streamlines study specific feasibility processes from site identification, performance analysis until contracting.
Assures that every study and all users are well-trained on the study before documentation can start. Optional test and re-trainings available. Documentation of trainings for quality purposes.
Designed to capture digital patient signatures on external devices (currently iOS / Android). Alcedis eConsent is compliant with data protection and regulatory requirements.
Drug accountability & sample tracking
Allows to always keep track on lab kit storage, sample shipment and supports drug accountability.
Simple organization of visits, standardized visit reports, great oversight with additional reporting features for protocol violations, open to-do's, transmission of follow-up letters etc.
Support via interactive online chat functionality within the eCRF.
Create individual laboratory templates including range checks for blood chemistry, hematology, coagulation or tumor marker within minutes.
Visual status control (traffic-light-system).
Alcedis eCRF includes a variety of standard reports for various processes.
Additional reports in standard formats like csv, xls etc. can be defined, configured and generated at any time via an intuitive interface.
Allows investigator or other defined roles to electronically sign case report forms. eSignature also delivers quick and helpful overviews of the signature status of patients' documentation.
Expand your eCRF within the Alcedis Platforms™
Powerful tools for all stakeholders involved
Safety & Compliance
Cover robustly all critical functions & processes
Speed & Costs
Reduced set-up timelines and maximum cost efficiency