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WEB DEMO
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WEB DEMO
  • Home
  • About
    • Our Story
    • Why CRFweb?
    • Contact
      • Our locations
      • Europe – UK Office
      • India
    • Security and compliance
  • Solutions
    • The EDC process
    • eCRF
    • MedDRA
    • Randomization
    • ePRO
    • eDiary
    • Innovations Hub
  • Sectors
    • Medical Devices
    • Pharma-Biotech
    • CROs
    • Academia
    • Nutraceuticals
  • Resources
    • News

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 "

Elisabeth Liljensten, CEO, Devicia AB

" As a leading Medical Device CRO, we understand the importance of a specialist EDC application in today’s market. I have no hesitation in recommending CRFWEB to our clients."

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."

Next Steps

For a quick system overview, click here

Seeing is believing. Book a web-based demo now.

Book a demo

Useful Links

  • eCRF
  • eDIARY
  • ePRO
  • MedDRA
  • Randomization
  • Security and compliance

Latest News

January 4, 2021

TO A BRIGHT NEW YEAR

Read more
June 3, 2020

Paper trials V EDC – what’s more cost-effective?

Read more
May 5, 2020

In a bit of a jam? How we’re keeping trials running

Read more

CRFWEB is a clinical trial software application by Clindox

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