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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
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      • technologies for medical device clinical trials
      • ePRO & eDiary for medical device clinical trials
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Articles
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Meeting the IVDR challenge: digitizing the collection of study data

June 20, 2022
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mike oxlee

Covid-19: What has been the impact of the pandemic on India and how have Indian Clinical Trials been affected?

March 14, 2022
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mike oxlee
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Decentralized Clinical Trials – new kid on the block or a venerable idea resurrected?

January 18, 2022
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mike oxlee
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Announcing the all New Clindox App

January 18, 2022
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mike oxlee
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Farewell 2021: A challenging year but successful for Clindox

December 21, 2021
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mike oxlee
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The Secret Clinical Affairs Director’s Christmas Wish List: plugging the EDC/CTMS technology gaps

December 16, 2021
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mike oxlee
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The true impact of MDR: a Clinical Affairs perspective

December 8, 2021
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mike oxlee
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Sustaining profitable market access under MDR: the PMS & PMCF business case for EDC

November 26, 2021
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mike oxlee
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Changes to IVDR: the irresistible force of the Commission bested by the immovable object of Reality

November 16, 2021
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mike oxlee
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MedTech Clinical Investigations. An essential guide to working with CROs and FSPs

November 9, 2021
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mike oxlee

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