DISTILL EDC
Take control of your clinical studies
DISTILL EDC system gives you back control of your clinical trials, allowing you to develop and manage every aspect from start to finish. DISTILL was developed by users to overcome the restrictions and costs associated with legacy systems.
DISTILL EDC
Take control of your clinical studies
DISTILL EDC system gives you back control of your clinical trials, allowing you to develop and manage every aspect from start to finish. DISTILL was developed by users to overcome the restrictions and costs associated with legacy systems.
Why wait for weeks for developers to focus on your project when you can do it yourself ?
DISTILL puts you in control
Run clinical trials efficiently, which simplify your electronic data capture and management
Save time and costs when setting up trials. Expedite mid-study changes in no time
Requires no specialist programmers or programming knowledge
Drag and drop user interface for trouble-free form design and customisation
User-friendly query builder suitable for creating advanced form logic sequences
The pursuit to better healthcare never waits…. neither should your clinical trials
Empowering you with the right insight,
through enhanced data management
Run clinical trials efficiently, simplify your electronic data capture and management
Data Uploader
User acceptance testing, training and live environments
Source data verification
Comprehensive reports, logs & dashboards
Data at your fingertips… to get it right first time
PERSONALISED PRICING TO FIT YOUR NEEDS
Pricing that gives you peace of mind
Simple pricing structure, with no hidden or feature based charges.
No hidden charges
No feature based charges
Simple pricing structure
Integrate DISTILL into your CRO offerings, to increase productivity and reduce timelines for study set up and mid-study changes. The simple to use form studio, with drag and drop user interface, allows for trouble-free form design and customisation with no need for specialist programmers. Manage your data capture solutions in-house, by building eCRFs, with inbuilt validations and logic, without compromising data quality. SVMPharma will provide training and support, making you the experts with full control.
Suitable for all sizes and types of clinical trials, whether early phase or collecting real world data, we believe DISTILL is the right solution.
DISTILL BENEFITS
Take Control of Your Clinical Studies
Take back control of your clinical trial without the need for specialist programmers
Quick trial setup and in-study changes
Reduced need for expensive and time-consuming customisations
Rapid seamless setup user acceptance testing, deployment.
Cut down on manual data entry with the bulk electronic data uploader.
Customisable and flexible to meet changing needs
Rapid execution of in-study changes
Flexible document uploads, broadcast messages, custom signatures and user-friendly query mechanism
Fully customisable roles and permission settings
Notifications of form changes with a fully customisable email templates and triggers
Gain data driven insights into the performance of your trails with flexible report and comprehensive list of audit logs
SVMPharma Support
Onboarding, training and ongoing support
User focused case report form development to match study protocol
Get the support you need from a team of product specialists to make your team DISTILL experts
Form building services available, with project planning throughout
At SVMPharma we see ourselves as part of our clients’ teams when working on projects
Find the service and packages to meet your needs
DISTILL FEATURES
FORM STUDIO
Form studio has been designed to allow a trial/data manager to create electronic case report forms without the requirement of a programmer
Drag and drop form builder with pre-built templates
Setup form controls and edit checks within minutes, not days or weeks
Automatically generated annotated case report forms and trial configuration specifications
Support for version control
LOGIC BUILDER
Logic builder removes the requirement of a programmer to code logic and allows immediate user acceptance testing.
Unique tool that allows the construction of logic that can be used to define form workflows, form controls, and edit checks
Step by step user interface based approach to create form validations, monitoring and logic
Wide range of customisable options which reduce the need for programming
FORM PUBLISHER
Move changes through design, user acceptance testing, training and live environments at the click of a button.
Publish changes to user acceptance testing, training and live environments with ease.
Changes are available immediately to any environment improving turn around times for user acceptance testing and training.
CONTENT MANAGEMENT
Fully customisable content management, stored in one place configurable to be viewed where needed
This includes help files, supporting documents, terms and conditions, custom email notification and form lock/sign/source data verification signature
Changes take effect immediately rather than taking days
USER ROLES AND PERMISSIONS
Fully customisable roles and permission settings
Add modify or disable user roles as per study requirements.
Individual role types can be configured to allow or restrict any feature within DISTILL
DATA UPLOADER
Electronic notes and prescribing records are a valuable source of data available for clinical trials that can be uploaded directly into DISTILL
Smart uploader that checks for data discrepancies before upload, so you spend less time fixing erroneous data
Reduce time for data entry, upload data directly in to electronic case report forms
Allows for uploading of hundreds and thousands of electronic records
Significant reduction in data entry by allowing data to be uploaded in bulk
FLEXIBLE REPORTS AND DASHBOARD
Real-time data enhances the efficiency of trial management. Allowing users to make informed decisions
User developed clinical trial key performance indicators
Real-time data tracking dashboard for clinical research organisation and sponsor
Data extracts available real time
Create custom reports and visualise data through the DISTILL dashboard
Real-time, automated, email notifications
COMPREHENSIVE LOGS
Provides full accountability of user activity within DISTILL through a comprehensive list of audit logs
Access to over 50 audit logs, that allow close monitoring of DISTILL activity
All files imported and exported, from DISTILL, can be traced a unique reference IDs
SOURCE DATA VERIFICATION
Built in source data verification modules
Electronic case report forms reviewed and signed at appropriate form stages
Pre-define source data verification fields
STUDY ARCHIVE
Generate end of trial PDF exports of all DISTILL data with ease
All patient data including form data, audit logs and queries easily exported to PDF for use in study archiving
Optional password protection, for clinical trial archive materials
Convenient bookmarks for individual files, so you can find the information you want quicker
INDUSTRIES WE SERVE
DISTILL is flexible for all clinicals studies and in every clinical setting
Biotech & Pharma
We offer clinical research organisation services and understand the increased need in biotechnology and pharmaceutical industries for rapid, seamless, setup of clinical trials, without compromising quality.
CROs
DISTILL provides the opportunity for CROs to take control of their clinical studies and offer their clients enhanced value
Academic Research
DISTILL provides high quality data capture solutions, which are cost effective and without the requirement of specialist programmers.
