Medical Coding – Integrated MedDRA

Code directly into your study with CRFWEB‘s integrated MedDRA

Dictionary coding is a regulatory necessity for many clinical trials and an advantage for many more. The clear market leaders in this area with the broadest recognition are MedDRA (Medical Dictionary for Regulatory Activities)

CRFweb has MedDRA coding integrated into our EDC database application and offers the following key functionality:

This is complementary with CRFweb. You will need your own MedDRA license, we will validate this for you, and you are then free to use it as part of your study as long as you maintain your Licence. You can make your next clinical study, a MedDRA clinical trial with CRFweb.

Features

Medical coding directly into your study with our MedDRA clinical trial module
Dictionary version available to match your license
Auto and manual mapping of MedDRA codes

Easy to use eCRF browser to search code at all levels
Export the coded study to PDF
Map live as investigator, or retrospectively as a data manager/monitor

5 Star Reviewed

What our clients say

Maria Galligan, PMD Solutions

" The Clindox team have been an incredible support and are always available to help in any way they can."

Dr Salvi, CRF Health, India

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

Nigel McLean, Cytosystems, UK

" CRFWEB eCRF, plus their helpful and accommodating staff, helped us quickly set up and personalize, with quick turn-around times of modifications, exactly what we, the clinical staff, and statistical consultants demanded, all at an affordable price "

Kelly Seamans, Atlantia

" The Clindox (CRFWEB) team are dedicated and enthusiastic about accommodating the unique requirements of each individual study and are great value for money."

Dr Satish Kumar, G7 Synergon

"Our international CRO business has utilized Clindox's integrated randomization module and Kit Management. The functionality provides everything we need, and having key trial components integrated into one system is a huge advantage to us in terms of trial efficiencies. Having both randomization and kit management capabilities, aligned with the EDC really simplifies the whole process and significantly reduces the time and effort required to manage our studies and keep control of our processes and inventory. "

Next Steps

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