Contact Us

If you still have questions or prefer to get help directly from an agent, please submit a request.
We’ll get back to you as soon as possible.

Please fill out the contact form below and we will reply as soon as possible.

  • Contact Us
  • Home
  • CDMS
  • Frequently Asked Questions
  • Collecting data

What to do if a subject withdraws consent?

Contact Us

If you still have questions or prefer to get help directly from an agent, please submit a request.
We’ll get back to you as soon as possible.

Please fill out the contact form below and we will reply as soon as possible.

  • CDMS
    Castor CDMS Manual Castor CDMS Calculations Manual Frequently Asked Questions Articles for Data Managers Castor CDMS Compliance Release Documents
  • eConsent
    Castor eConsent Manual Castor eConsent Compliance Release Documents
  • SMS
    Castor SMS Manual Castor SMS Compliance Release Documents
  • Castor Connect
    Castor Connect Compliance Release Documents Castor Connect Manual Castor Connect - Participant Quick Start Guide
  • Helpdesk
    News Other Resources Castor products knowledge resources
  • Status page
  • Completing a Study
+ More

If a subject withdraws consent, follow the forms below:

  1. Lock the participant or parts of the participant which should no longer be modified
  2. Make sure to trigger an exclusion message - these can be set up in the Data validation tab for a field
  3. Archive the participant - archived participant will not be visible in the data entry and will not be exported. You can unarchive a participant at any time.

Note: If a patient withdraws from the study before they have completed all visits, then these underlying forms can be marked as user missing. You can also import user missing data. Alternatively, you may choose to hide visits with the automation engine. Please note that one field can only trigger one automation at a time.

subject withdrawal consent withdrawal

Was this article helpful?

Yes
No
Give feedback about this article

Related Articles

  • Why can't I open/enter my study?
  • How to lock a participant to prevent further data entry
  • Can I gather data for multiple research centers?
  • What is the maximum length of text for fields and options?
ISO 27001
FDA - 21 CFR part 11
ICH GCP compliant
HIPAA compliant
CDISC
ISO 9001
gdpr compliant

Products & Industries

  • Electronic Data Capture (EDC)
  • ePRO
  • eConsent
  • Decentralized Clinical Trials (DCT)
  • Clinical Data Management
  • Medical Device & Diagnostics
  • Biotech & Pharma
  • CROs
  • Academic Research

Resources

  • Thought Leadership
  • Blog
  • Castor Academy
  • Knowledge Base

 

Company

  • About Us
  • Careers
  • News
  • Contact Support
  • Contact Us

Legal & Compliance

  • Terms of Use
  • Privacy & Cookie Statement
  • Responsible Disclosure Policy
  • Good Clinical Practice (GCP)
  • ISO Compliance Certificates
  • GDPR & HIPAA Compliance
  • Security Statement

© 2022, Castor. All Rights Reserved.

Follow us on social media


Knowledge Base Software powered by Helpjuice

Definition by Author

0
0
Expand