Why are we different?

Simplifying functionality in real world studies

We Improve productivity for Pharma by reducing the burden on doctors. Our unique focus on PMS studies has enabled us to simplify the collection and management of patient data– giving rise to a range of benefits that place RealWorld EDC ahead of other choices.

RealWorld EDC is the only CDISC certified and FDA compliant electronic data capture system that is specifically developed for post-marketing surveillance (PMS) studies.

RealWorld EDC provides numerous Benefits

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Save time for busy doctors

It's intuitive interface and reduced functionality makes it easy to use - therefore reducing demands on clinic time.

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Study design flexibility

We can tailor eCRFs to suit your specific study.

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High-quality data at a cost-effective price

We don’t compromise on quality.

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Multi-language capability

Available for all languages.

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CDISC Certified & FDA compliant

We recognize the importance of complying with the global gold standard for medical research.a

Additional benefits include

EXPERIENCED EDC PROVIDER

We have worked with world leading pharmaceutical companies who have testified to their positive experiences with RealWorld EDC.

ASSURED QUALITY AND COMPLIANCE

As an experienced CDISC certified and FDA complaint EDC provider we adhere to global regulatory standards.

FASTER SET-UP TIME

Our standardised RealWorld Study Builder means studies can be set up quickly, shortening time to study completion

CONTINUALLY DEVELOPED WITH INPUT FROM CLIENT

Our solution has been developed with input from doctors, nurses, patients, pharma and CRO clients enabling us to optimise PMS studies for the end user.

COUNTRY SPECIFIC DIFFERENCES RECOGNIZED

We have a comprehensive understanding of varying legislations across different global markets and take account of this in study design.

To find out how RealWorld EDC can transform your companies PMS studies contact us now

Get in touch

Don’t hesitate to contact us. Our experts would love to help you transform your company’s post-approval studies with our software.

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