DISTILL Technologies LLC 3701, Churchill Executive tower, Business Bay, Dubai, UAE

DISTILL EDC

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DISTILL EDC

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 following the guidelines of users from 4 major pharma companies. DISTILL overcomes the restrictions and costs associated with legacy systems.

DISTILL BENEFITS

Take Control of Your Clinical Trials

Don’t wait weeks for programmers to be ready for you. Reduce time in form building and managing clinical trials, including mid-study changes. Rapid seamless setup, UAT, training and deployment, all under your control. 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 fully customisable email templates and triggers. Gain data driven insights into the performance of your trials with flexible reports, graphs and comprehensive list of audit logs. 

SVMPharma Support

Onboarding, 12 hours of initial training and monthly ongoing support included. 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.

Why wait for weeks for developers to focus on your project when you can do it yourself ? DISTILL puts you in control.

Save time and costs when setting up trials. Expedite mid-study changes in no time

It will also help to increase productivity and reduce timelines for study set up and mid-study changes. Form studio is super easy to use, with drag and drop user interface, it allows for trouble-free form design and customisation with no need for specialist programmers. Manage everything in-house, by building eCRFs, with inbuilt validations and logic, without compromising data quality. DISTILL will provide training and support, making you the experts with full control.

Suitable for all sizes and types of clinical trials, drugs and medical devices, whether early phase or collecting real world data, DISTILL is the right solution.

Compliance and Security

DISTILL EDC is fully compliant, secure and follows all of the necessary protocols, and even a few extra just to be certain. We adhere to the strictest of standards and meet or exceed all global data collection regulations such as 21 CFR 11 ICH/GCP, GDPR, and HIPAA. DISTILL allows you to focus on your clinical trial with complete confidence that your data is compliant & secure.

DISTILL is flexible for all clinicals studies and in every clinical setting.

Biotech & Pharma

We understand the increased need in biotechnology and pharmaceutical industries for rapid, seamless, setup of clinical trials, without compromising quality. This is what DISTILL is all about.

CROs

DISTILL provides the opportunity for CROs to take control of their clinical studies and offer their clients a cost effective alternative to legacy EDCs. Integrate DISTILL into your CRO offerings, not to replace your current EDC partners, but to offer a more affordable alternative to your low budget customers. Benefit from volume discount licenses.

Academic Research

DISTILL provides high quality data capture solutions, which are cost effective and without the requirement of specialist programmers. Ask us about our special non-profit / academia / Investigator driven studies discounts.