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

Benefits of RealWorld EDC

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Saves time for busy doctors

It’s intuitive interface and reduced functionality makes it easy to use. Doctors can learn to use RealWorldEDC in about 15 minutes thus reducing demands on clinic time. It’s ease of use also results in fewer support calls and less monitoring visits.

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Study design flexibility

We offer study specific adaptability whereby we can tailor eCRFs  to suit your  study needs.

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High Quality data at cost effective price

We don’t compromise on Quality; we offer regulatory compliant EDC at a reasonable cost.

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Multi language capability

RealWorld EDC has built-in support for multiple languages, making it much easier to run studies across multiple countries in local languages.  While most EDC systems translate the eCRF only; RealWorld EDC translate the entire system including online instruction and edit checks.

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

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

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with our experts today to see how our software can transform your company's post approval studies

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