Post-Market, Post-Approval Studies

Post-Approval-and-Post-Marketing-Research

CRFWEB‘s core attributes makes it the perfect option for post-approval or post-market research. Our super-fast, DIY set-up option and simplicity of use, makes it ideal for putting together studies where turnaround time is of the essence and flexibility is paramount.

  • Quick Set-up and rapid trial turnaround
  • Decentralised or hybrid trial ready with Direct Data Capture and subject-led Data capture 
  • Quick Set-up and rapid trial turnaround
  • Post-marketing studies, registries, safety, observational

Post-Marketing for Medical Devices

While CRFWEB is suitable for any post market studies, the MDR and IVDR regulations in Europe have upped the significance for medical devices in particular. If you want to market your medical device in Europe, you will need to meet compliance requirements, whether your appliance is new to market or already there. You will also need to provide ongoing evidence with respect to safety and efficacy.

With the ability to deliver subject-led data capture via the CRFWEB App,  our ePRO and eDIARY modules are of particular benefit to those looking at post market evaluation.

Contact us today to arrange a web demo and see how we can assist your post market evaluations.

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

For a quick system overview, click here

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Latest News

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