Good Clinical Practice Guide
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Forum: Investigator Sites (inc Principal Investigator responsibilities, consent, source data and CRFs)

  1. Sticky Thread Sticky: MHRA produced FAQs for Investigator Sites

    Started by MHRA Super Moderator, 14th Oct 2011 10:58 AM
    • Replies: 4
    • Views: 23,889
    2nd May 2013, 03:34 PM Go to last post
  1. Subjects date of consent

    Started by Trialblazer, 7th Aug 2017 02:25 PM
    • Replies: 1
    • Views: 4,527
    15th Sep 2017, 07:46 PM Go to last post
  2. Submission of PI for FIH studies application

    Started by Natasha, 29th Jul 2015 10:06 AM
    • Replies: 1
    • Views: 10,241
    29th Jul 2015, 12:09 PM Go to last post
  3. SUSARs sent to pharmacies

    Started by Nikki Dewick, 23rd Oct 2015 12:43 PM
    • Replies: 0
    • Views: 24,149
    23rd Oct 2015, 12:43 PM Go to last post
  4. Translator signing ICF as a witness

    Started by MonitorH, 3rd Sep 2012 01:17 PM
    • Replies: 1
    • Views: 5,843
    4th Sep 2012, 09:34 AM Go to last post
    • Replies: 1
    • Views: 10,902
    11th Jun 2013, 04:30 PM Go to last post
  5. ‘Re-consenting’ trial participants

    Started by SRH, 24th May 2012 11:24 AM
    • Replies: 3
    • Views: 19,264
    23rd Dec 2017, 11:20 AM Go to last post

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