CRFweb

The CRFWEB team’s focus and experience in medical device investigations means our eClinical platform provides all the tools you’re likely to need to meet your regulatory requirements

CRFWEB will also provide you with the opportunity to discover new scientific, technical and operational insights derived from your data

Details ➡️ https://crfweb.com/medical-devices/

The data capture element within CRFWEB is a simple process

Users are taken through a step by step process for data entry and you can save and review saved work as you go

You can find out more about data capture within CRFWEB on our website

Data Capture ➡️ https://crfweb.com/the-edc-process/

If you are interested in what CRFweb can do for you, why not book a demo?

Just fill out the form on our website, and we’ll schedule a live demo of CRFWEB at a time that suits you

Book A Demo ➡️ https://crfweb.com/request-a-demo/

The Innovations Hub is where we showcase what's available for testing and coming soon to CRFWEB

For more information on products/modules in our development pipeline, visit the hub on the link below

Innovations Hub ➡️ https://crfweb.com/innovations-hub/

CRFWEB helps companies capture data from clinical trials more easily, efficiently and cost-effectively

To find out more about CRFWEB and its benefits, take a look at our website

Why CRFWEB ➡️ https://crfweb.com/why-crfweb/

The CRFWEB EDC application enables you to create eCRFs, and provides everything you need to put together a compliant investigation, helping you do it in the most efficient way possible

To find out more about EDC within CRFWEB, take a look at our website

EDC ➡️ https://crfweb.com/technology-medical-device-clinical-trials/

Introducing the Secret Clinical Affairs Director

By maintaining anonymity, our highly experienced Clinical Affairs professional speaks candidly and provides some really fascinating insights about how the new regulatory regime will impact the market for medical devices in Europe over the coming years

Read ➡️ https://crfweb.com/impact-of-mdr-on-med-tech-clinical-affairs/

With CRFWEB, a study can be designed to be entirely ePRO

It is also possible for a particular visit within a study to be designed as ePRO, giving ultimate flexibility in study design

ePRO ➡️ https://crfweb.com/epro/

The randomization module within CRFWEB is comprehensive and highly flexible

This includes simple, block, stratification and adaptive methods, all of which are fully integrated into CRFWEB's EDC or as a standalone module

Randomization ➡️ https://crfweb.com/randomization/

With CRFWEB, you can medical code directly into your study with our MedDRA clinical trial module

The easy to use eCRF browser allows users to search code at all levels, and export the coded study to PDF

MedDRA ➡️ https://crfweb.com/meddra/

Core to CRFWEB is an electronic case report form or eCRF software application which forms the hub of our system

All of our features are available from one simple dashboard, making our eCRF software application the system of choice for your next study

Details ➡️ https://crfweb.com/ecrf/

The process for designing a study collecting the data, managing that data and reporting on it is straightforward and logical in the CRFWEB application

You can find out more about the EDC process on our website using the link below

EDC Process ➡️ https://crfweb.com/the-edc-process/