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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

Coronavirus Statement

Open for Business With Operational Changes

We recognize the situation with Covid-19 is a dynamic one and that challenges lie ahead for our clients in fulfilling their study requirements. As an EDC supplier we have been working hard behind the scenes to ensure that we can continue to provide fully operational customer service for our clients and at the same time ensure that we continue to meet stringent requirements regarding data security and compliance. All our staff are now working remotely from home using secure connections. Rest assured that all appropriate measures are in place and we can continue to operate securely and at full capacity.

 

Assisting Our Clients Working From Home

We recognise that working from home may also have an impact on our client’s working practices. Should anyone have any difficulties connecting to the CRFweb system for any reason please contact us via the details below and we will be happy to assist. 

email: crfwebsupport@clindox.com

tel: +91-20-71531039

Chat facility: click here

 

Helping Clients Find New Ways to Collect Data – ePRO and eDiary offer

With many countries in lockdown, these difficult times make traditional methods of data collection unviable. There is however a potential alternative. Our ePRO and eDiary modules can be added to existing studies to allow subject-led data entry. These modules can be used on their own for standalone studies but an existing eCRF can also have visits added/amended to eDiary or ePRO.

Normally, these modules are an added extra but we are offering all our customers the opportunity to use ePRO/eDiary for free on any current study or included in the cost of the base eCRF on any new study until further notice. Please contact our customer service team for a demonstration or further details.

Tom Beaufoy, CEO

Whether it’s to take advantage of the move towards decentralised clinical trials, to facilitate patient reported outcomes or simply to speed up patient recruitment and increase engagement, eConsent is an ever more critical tool in the clinical trial management process.

Like all our modules, eConsent is seamlessly integrated into the CRFWEB application. Subject data can be captured instantly online or offline and synced when a secure connection is available.

eConsent Features

Options for eSignature include:

  • fingerprint recognition
  • signature touchscreen collection
  • subject video
  • geo-location and timestamp

Options to enhance engagement include the facility to add content including:

  • images, videos, questionnaires.

CRFWEB eConsent makes appropriate checks to ensure consent is provided before any study data is collected.  The result is a compliant and secure process to enable subject sign up and help improve both sign up and retention rates.

5 Star Reviewed

5 Star rated on Capterra

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

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

Book a demo

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

Read more
March 14, 2022

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

Read more
January 18, 2022

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

Read more

5 Star rated on Capterra

CRFWEB is a clinical trial software application by Clindox

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