Why choose CRFweb?

Why choose CRFweb?

Capture data for clinical trials easily, efficiently, securely, compliantly and do it in days not weeks or months.
It’s a fraction of the cost of the ‘industry big names’ without compromising on functionality. No hidden extras.
Choice. We will build the study for you or mentor you through your own build.
A partner not a supplier. Your own dedicated support representatives will guide and assist you every step of the way.

Client Testimonials

Client Testimonials

"As a leading Medical Device CRO, we understand the importance of a specialist EDC application in today’s market. I have..." Read More

Elisabeth Liljensten, CEO, Devicia AB

"We’re very happy we chose CRFweb. We now feel we have greater control over our trial management process, our trials..." Read More

Maria Galligan, PMD Solutions

"The time and cost saving is really significant. We're very happy with the performance of CRFweb and I wouldn't hesitate to..." Read More

Dr Salvi, Chest Research Foundation, India

"Clindox are dedicated and enthusiastic about accommodating the unique requirements of each individual study and are great value for money.Read..." Read More

Kelly Seamans, Atlantia

"Cytosystems is running a multi-centered clinical performance evaluation study for its proprietary urine based diagnostic for bladder cancer.  We require..." Read More

Nigel McLean, Cytosystems, UK

"After a thorough review of the marketplace and extensive testing, I decided to propose CRFweb to my clients.  Their team..." Read More

Dr. Manish Rajak , Innvocept Solutions, India
crfweb for BA/BE

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The EDC process

The EDC process


Products and Features

The EDC process



CRFweb is an EDC (Electronic Data Capture) application for clinical trials. Core to the proposition is an electronic case report form or eCRF which forms the hub of the application. The key ethos behind CRFweb is integration and consequently all our other functionality integrates with the CRF

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CRFweb now features a fully integrated ePRO (electronic patient reported outcome) interface, where subjects can answer questionnaires without risk of accessing other functionality or data. Site staff can easily initiate a subject session to allow the subject to answer at the clinic (e.g. using a tablet), or the subject can log in from home with a unique username and password. A study can be designed to be entirely ePRO. It’s also possible for a particular visit within a study to be designed as ePRO, giving ultimate flexibility in study design. With data entry by the subject, both ePRO and the complimentary eDiary module, lend themselves especially well to post-market studies. In addition to the obvious time and cost saving benefits, there is also the benefit of increased patient engagement in the whole trial process. Features summary: Multilingual patient questionnaires/surveys Easy switch to subject entry mode Subject login from home Data entry on tablet No risk of subject accessing other functionality or data Scheduling and reminder facility.

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Like all features of CRFweb, the eDiary function is integrated into the application. Working alongside our ePRO functionality, eDiary allows greater interaction with the subject through login via mobile device for daily observations and improving data collection response through reminders and alerts. Core functionality: Prepare a schedule / calendar for data capture and assign subjects intended to be part of the study Login through Android / iOS devices to record daily observations Complex formulas and edit checks to manage the study complexity Notification to investigators/Nurses to visit Subject on any observations during data capture No risk of subject accessing other functionality or data Notification/Alerts to Subject for any data which needs quick action by Subject eg Visit to Doctor, Nurse, etc For a demo please fill in our demo request form or call for further information.

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Dictionary coding is a regulatory necessity for many trials and an advantage for many more. The clear market leader in this area with the broadest recognition is MedDRA (Medical Dictionary for Regulatory Activities). CRFweb has MedDRA coding integrated into our application and offers the following key functionality:

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CRFweb offers simple, block and stratified randomization. The randomization module allows clients to randomize subjects in two way. Option 1 allows for randomization as a group of subjects in circumstances where all subjects are known. This allows for sampling and control groups according to requirements. Option 2 is to randomize ‘on the fly’. Allowing treatment groups to be randomly assigned to a subject by the investigator in real time.

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CRFweb has integrated electronic Trial Master File (eTMF) functionality. This enables clients to; Manage eTMF documents Group the eTMF documents Upload the documents or images for a particular study Share study protocol document to users of a study Full feature WYSIWYG (What you see is what you get) editor for adding details Access questionnaire and licence requirements and validate the same Please call or fill out our web demo request form to find out more about our integrated eTMF.

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Medical Device Investigations

The End of Paper-based Trials?

Medical equipment on table. Blue stethoscope and tablet on white background.

Market-tested. Proven. Cost-effective EDC.

Currently helping medical device companies meet their business and compliance requirements.

The End of Paper-based Trials?

The End of Paper-based Trials?

Is this ‘ The End of Paper-based Trials? ’ Download our feature on the four reasons why companies still use paper-based trials… and why they no longer need to

Latest News

CRFweb Latest News