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  • BADBIR
  • Participants
    • Using the Patient Portal
    • Your data
    • Participant FAQs
    • Patient Newsletters
  • Clinicians
    • Eligibility
    • Study information
      • Conducting BADBIR remotely
      • Associate Principal Investigator Scheme
      • Centre Report
      • Average daily dose
      • Participating centres
      • Steering Committee & DMEC
      • Stop reasons
      • Study FAQs
    • Baseline and follow-up
    • Adverse Events (AE) and Events of Special Interest (ESI)
      • ESI forms
    • Patient Portal information for clinicians
    • How we use your data
    • Database
      • Register for a database account
      • Database help
        • Training
        • Avoiding data queries
        • Registering a new patient
        • Sending us a consent form
        • Database FAQs
      • How PIs can register new research team members
    • Useful resources
  • R&D
    • Site file documents
      • Superseded documents
      • Amendments
      • Ethics progress reports
    • Study payments
    • Clinical Research Networks
  • Data and publications
    • Publications
      • Guidance for publishing BADBIR findings
    • Using BADBIR data
      • Data access FAQs
  • News
    • Centre Recognition Award
    • Newsletters
    • Patient newsletters
  • Contact
  • Patient Portal
  • Clinician Database

Ethics Progress Report: 2012

by Web team (HR) | Jun 21, 2012 | Ethics Progress Reports | 0 comments

Read the 2012 Ethics Progress Report.

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