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WEB DEMO
  • Home
  • About
    • Our Story
    • The Executive Team
    • Why CRFWEB?
    • Contact
      • Our locations
      • Europe – UK Office
      • India
    • Careers
    • Security and compliance
  • Solutions
    • The EDC process
    • eCRF
    • MedDRA
    • Randomization
    • ePRO
    • eDiary
    • The Clindox App
    • Clindox eLab
    • Innovations Hub
  • Medical Devices
    • Medical Devices Home
    • Introduction to Medical Device Investigations
    • Pre-Licence Investigations
    • Post-Market Investigations
    • Technologies for Investigations
      • technologies for medical device clinical trials
      • ePRO & eDiary for medical device clinical trials
      • EDC for medical device clinical trials
      • The Clindox App for medical devices
      • Clindox eLab
    • Medical Device Regulations
    • Medical Device Resource Centre
    • Clindox for IVD Studies
  • Other Sectors
    • Pharma-Biotech
    • Nutraceuticals
    • CROs
    • Academia
    • Clindox for IVD Studies
  • News
Articles
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We have a brand new UI… and we’re just a little bit proud of it!

April 19, 2021
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mike oxlee
Articles
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TO A BRIGHT NEW YEAR

January 4, 2021
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mike oxlee
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Paper trials or EDC – what’s more cost-effective?

June 3, 2020
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mike oxlee
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CRFWEB to the Rescue

May 1, 2020
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mike oxlee
ePRO
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It’s been a productive year for the CRFweb team

December 18, 2019
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james blundell
Post-Approval-and-Post-Marketing-Research
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Approaches for reducing clinical trial costs – why are we still using paper?

July 4, 2019
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james blundell
Beat the clock to medical device compliance
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Beat the clock to medical device compliance

March 30, 2019
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james blundell
Post-Approval-and-Post-Marketing-Research
Articles
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The end of the paper trial?

March 4, 2019
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james blundell
MEDICAL-CODING
Articles
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Reaping the Benefits of Medical Coding

February 19, 2019
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james blundell
Compliance
Articles
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Compliance and edc systems in clinical trials

February 19, 2019
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james blundell

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