EMPOWERING HEALTHCARE DECISIONS AROUND THE WORLD

Simplifying the collection of patient data in the real world

REAL WORLD EVIDENCE

How a drug impacts patients’ lives in a real-life setting is empowering healthcare decision making around the world.

By listening to our customers we realised that the process of capturing this data in the Real World setting is time - consuming for busy doctors.

So, for over a decade we have developed an easy to use Electronic Data Capture - EDC - application specifically for Post Marketing Surveillance - PMS - studies.

7,000 patient study: RealWorld EDC User Experience

RealWorld EDC Survey Russia

Survey Results from 462 Doctors who used RealWorld EDC

462 out of 700 doctors completed a survey about their experience
using RealWorld EDC in Russia.

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15

Minutes to train Doctors

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92%

Doctors said they would use it again

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2%

Helpdesk Calls

(347 calls out of 21,000 patients)

Since 2003 we have developed an easy to use Electronic Data Capture (EDC) application specifically for Post-Marketing Surveillance(PMS) studies. It has been used in over 70 studies with more than 20 Pharma companies and CRO.

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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.

“The support provided has been over and above what was expected. CTEPs understanding of the NIS arena and their contact has been exceptional”.

Project Manager, Astellas

“… very professional, helpful and responsive…”

"..well done to you and CTEP on the very professional approach and getting such a good application in on time …..and particularly the follow up on the queries."

MD, Novartis

“There is no doubt that CTEP resources in progressing have been of great assistance our local clinical trial programmes over the years.”

General Manager, Roche

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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