Meet the MDR revised deadline with CRFWEB‘s all-inclusive compliance package.

The recently proposed extension of the deadline for MDR to 26 May 2021 has bought some time for businesses seeking to gain approval for their devices.

This is a great opportunity to achieve compliance. But you need to start NOW!

Why choose the CRFWEB

all-Inclusive compliance package?

1. Meet your regulatory requirements:

MDR Compliance

FDA Compliance

GDPR Compliance

2. Meet your business requirements:

Beat the deadline

Start Now, and meet the revised May 2021 deadline.

Fixed Price

One fixed price. No extras. Fix your budget for compliance.

All-Inclusive Package

No limit on sites or subjects. No set-up fee, we set up for you. Choose any of our EDC tools you need.

Plus all the data capture and management tools you need – in one package

eCRF

Get full control of electronic data capture (EDC) collection, processing, monitoring, and reporting.

eDiary

Prepare a schedule/calendar for subject-led data capture through the CRFweb app.

Randomization

Use our integrated module for simple, block and stratified randomization.

ePRO

Allow patients to easily collect patient-reported outcomes (PROs) on any device of their choice.

MedDRA

Embed medical coding directly into your study with our MedDRA clinical trial module.

eTMF

Seamlessly manage, group, upload and share study protocol documents.

Contact our team for further details:

What Our Customers Say

Maria Galligan, PMD Solutions

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

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 "

Take the vital first step now to secure compliance. Contact us today.

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