Good Clinical Practice Guide
Page 3 of 3 FirstFirst 123
Threads 61 to 65 of 65

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: 23,613
    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: 4,361
    15th Sep 2017, 07:46 PM Go to last post
  2. Filing in patient notes

    Started by wigs, 9th Feb 2017 04:18 PM
    • Replies: 2
    • Views: 8,261
    22nd Feb 2017, 02:49 PM Go to last post
    • Replies: 1
    • Views: 6,026
    19th Jan 2012, 11:55 AM Go to last post
  3. Fasting before Consent

    Started by ztarfizh, 26th Nov 2012 11:11 AM
    • Replies: 2
    • Views: 7,546
    27th Nov 2012, 03:58 PM Go to last post
  4. Documenting SAE causality in source data

    Started by ztarfizh, 7th Apr 2014 03:23 PM
    • Replies: 4
    • Views: 15,710
    6th Aug 2015, 09:51 AM Go to last post

Page 3 of 3 FirstFirst 123

Forum information and options

Moderators of this Forum

Thread Display Options

Use this control to limit the display of threads to those newer than the specified time frame.

Allows you to choose the data by which the thread list will be sorted.

Order threads in...

Note: when sorting by date, 'descending order' will show the newest results first.

Icon legend

Contains unread posts
Contains unread posts
Contains no unread posts
Contains no unread posts
More than 15 replies or 150 views
Hot thread with unread posts
More than 15 replies or 150 views
Hot thread with no unread posts
Closed Thread
Thread is closed
Thread Contains a Message Written By You
You have posted in this thread

Posting Permissions

  • You may not post new threads
  • You may not post replies
  • You may not post attachments
  • You may not edit your posts
  •