SVMPharma’s mission is to provide unique technology which shifts the paradigm, in clinical research, at the same time maintaining simplicity with greater control for researchers

WHO WE ARE

Generating the Outcomes that Matter

At SVMPharma we have a passion for clinical research and ‘outcomes that matter’ to our clients. We provide accessible electronic data capture solutions, allowing you to operationalise your clinical trials, and take back control.

SVMPharma has come from a CRO background, delivering clinical trials for pharmaceutical and biotechnology companies since 2014. This history and experience has led to the development and launch, in 2022, of DISTILL electronic data capture system. The system has been designed and developed by researchers, using the technological expertise of Solverminds Solutions and Technologies, to build a system which can be used by all, no need for a specialist programming team, DISTILL is a user friendly and flexible system and SVMPharma will be there to provide training and support to our clients throughout.

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DISTILL EDC

Take control of your clinical trials

DISTILL is a new EDC system that 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.

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DISTILL EDC

Take control of your clinical trials

DISTILL is a new EDC system that 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.

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

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Take back control of your clinical trial without the need for specialist programmers. Reduce time in form building and managing clinical trials, including mid-study changes. 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

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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. Reduced need for expensive and time-consuming customisations.

SVMPharma Support

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Onboarding, training and ongoing support available. 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

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Form studio has been designed to allow a trial/data manager to create electronic case report forms without the requirement of a programmer

Logic Builder

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Logic builder removes the requirement of a programmer to code logic and allows immediate user acceptance testing

Form Publisher

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Move changes through design, user acceptance testing, training and live environments at the click of a button.

Content Management

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Fully customisable content management, stored in one place configurable to be viewed where needed

User Roles and Permissions

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Fully customisable roles and permission settings

Data Uploader

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Electronic notes and prescribing records are a valuable source of data available for clinical trials that can be uploaded directly into DISTILL

Flexible Reports and Dashboard

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Real-time data enhances the efficiency of trial management. Allowing users to make informed decisions

Extensive Logs

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Provides full accountability of user activity within DISTILL through a comprehensive list of audit logs

Source Data Verification

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Built in source data verification modules

Study Archive

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Generate end of trial PDF exports of all DISTILL data with ease

INDUSTRIES WE SERVE

SVMPharma’s DISTILL is flexible and can be used in all phases and types of clinical trials and in every clinical setting

Biotech & Pharma

Rapid seamless setup of clinical trials, high quality data capture, management systems of the data and real time reporting

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.

ENDORSEMENTS

At SVMPharma we have always had a single minded goal to work with clients to build successful relationships and generate the outcomes that matter. However, do not just take our word for this

collons

I came across SVMPharma after reading a report about some work they had done in oncology – very impressive work that had affected a NICE decision. We met with SVMPharma and we are now engaged on a couple of projects with SVMPharma – working very closely. They facilitate the paperwork to allow data collection, become part of the cross-functional team driving results and bring a wealth of experience to the table too. SVMPharma has been a pleasure to work with and I would strongly recommend contacting them to get their input first-hand on real-world data.

European Managing Director
collons

…the experience so far has been very positive with good communication, open discussions and things being done to a high standard. [The client] was a bit sceptical to work with a small company at the start, but compared to global vendors he’s worked with in the past, SVM has ‘knocked them out of the park.

Medical Director
collons

[The study] will be an important benchmark for the future.

European Managing Director

PUBLICATIONS

2022 February

Retrospective analysis of real-world treatment patterns and clinical outcomes in patients with advanced non-small cell lung cancer starting first-line systemic therapy in the United Kingdom

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2022 February

Real world outcomes in platinum sensitive relapsed ovarian, fallopian tube, or peritoneal cancer treated in routine clinical practice in the United Kingdom prior to poly-ADP ribose polymerase inhibitors

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2022 February

A treatment evaluator tool to monitor the real-world effectiveness of inhaled aztreonam lysine in cystic fibrosis

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2022 February

Effects of Initiating or Switching to a Six-Monthly Triptorelin Formulation on Prostate Cancer Patient– Healthcare Interactions and Hospital Resource Use: a Real-World, Retrospective, Non-Interventional Study

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2022 February

Aztreonam Lysine (Cayston)

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