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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

CRFWEB – EDC for Nutraceutical Clinical Studies

eTMF
  • Fast-to-Set up, slick user interface

    Set-up yourself or we’ll do it for you. Perfect for trials with a quick turnaround

  • All the features you need at sensible pricing

    Randomization and Medical coding all integrated. SDTM reporting.

  • Direct Data Entry and subject-led data entry if required.

    The CRFWEB App facilitiates CRC direct data capture or subject-led eDiary or ePRO. Ready for decentralised or hybrid trials if required.

Why use EDC for nutraceutical clinical studies?

Why use EDC for Nutraceutical clinical studies? Beverage studies and ingredient and supplement clinical trials are typically faster moving than their pharma or medical device counterparts. As such the ability to set up a study quickly, input date efficiently and then manage and report on that data are critical to facilitate a rapid turnaround. For these reasons, historically EDC systems have been avoided by the industry for nutraceutical studies, especially as budgets are also typically significantly less and compliance has been less onerous.

In simple terms, EDC can help streamline the food study process from start to finish saving a lot of time and money – whilst providing secure, manageable and reportable data in a timely fashion. Using an FDA compliant system built to GCP standards also helps ensure regulatory requirements are met. In the modern world, providing the solution is cost-effective, it makes no sense not to use EDC. But ideally, it needs to do everything you require it to, entirely in one integrated system.

Proven in the Market for Nutraceutical Clinical Studies

 

Naturally, you want an application for your nutraceutical studies that is proven in the field. CRFWEB, has been successfully delivering multiple clincial trials every year in the food sector for over 3 years.  Call us now for more details or request a demo.

Request Demo

5 Star Reviewed

5 Star rated on Capterra

What our clients say

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.

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Useful Links

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

Latest News

June 20, 2022

Meeting the IVDR challenge: digitizing the collection of study data

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March 14, 2022

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

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January 18, 2022

Decentralized Clinical Trials – new kid on the block or a venerable idea resurrected?

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5 Star rated on Capterra

CRFWEB is a clinical trial software application by Clindox

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