Good Clinical Practice Guide
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Threads 31 to 60 of 80

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: 128,955
    MHRA Super Moderator
    2nd May 2013, 03:34 PM Go to last post

  1. Image files as Source Data

    Started by ltebbs, 10th Nov 2011 05:36 PM
    • Replies: 1
    • Views: 6,265
    ashirve
    14th Nov 2011, 05:16 PM Go to last post

  2. Delegation of Duties

    Started by Jasper, 15th Apr 2012 03:29 PM
    • Replies: 1
    • Views: 30,369
    a123456
    12th May 2013, 07:52 PM Go to last post

  3. Phase I accreditation - physician resuscitation experience

    Started by ztarfizh, 30th Dec 2011 10:00 PM
    • Replies: 1
    • Views: 11,885
    MHRA Moderator
    19th Jan 2012, 11:55 AM Go to last post

  4. "Dictated" source data

    Started by LucCo, 22nd Jun 2012 08:20 AM
    • Replies: 1
    • Views: 7,384
    a123456
    22nd Jun 2012, 03:58 PM Go to last post

  5. Consent in Emergency Research

    Started by Hugh Davies, 2nd Oct 2012 02:41 PM
    • Replies: 1
    • Views: 72,654
    MHRA Moderator
    4th Oct 2012, 01:33 PM Go to last post

  6. Translator signing ICF as a witness

    Started by MonitorH, 3rd Sep 2012 01:17 PM
    • Replies: 1
    • Views: 33,482
    a123456
    4th Sep 2012, 09:34 AM Go to last post

  7. Patient Confidentiality and Data Protection

    Started by E.Atkin, 8th May 2013 11:04 AM
    • Replies: 1
    • Views: 16,311
    a123456
    10th May 2013, 10:13 AM Go to last post

  8. Question Independent Nurse Prescribers in Clinical Trials

    Started by Jasper, 17th Jul 2013 09:43 PM
    • Replies: 1
    • Views: 57,137
    a123456
    19th Jul 2013, 08:00 PM Go to last post

  9. Volunteers attending screening but not consenting

    Started by Research Coordinator, 7th Jun 2013 04:01 PM
    • Replies: 1
    • Views: 17,264
    a123456
    11th Jun 2013, 04:30 PM Go to last post

  10. Investigator CVs and GCP training

    Started by Speediepup, 2nd Jan 2014 03:35 PM
    • Replies: 1
    • Views: 184,301
    a123456
    4th Jan 2014, 12:46 PM Go to last post

  11. Reimbursement for patients time

    Started by klapsa, 27th Feb 2014 02:49 PM
    • Replies: 1
    • Views: 13,073
    a123456
    27th Feb 2014, 05:37 PM Go to last post

  12. Responsibility of PI when Study Archived

    Started by kate lees, 26th Jun 2014 08:00 AM
    • Replies: 1
    • Views: 17,740
    a123456
    27th Jun 2014, 10:41 AM Go to last post

  13. Redacted source documents

    Started by NAdey, 23rd Oct 2019 10:05 AM
    • Replies: 1
    • Views: 53,901
    a123456
    24th Oct 2019, 08:06 PM Go to last post

  14. Sub/Co-Investigator absence and delegation of authority

    Started by smezzian, 19th Jul 2021 06:25 PM
    • Replies: 1
    • Views: 16,049
    a123456
    5th Aug 2021, 03:08 PM Go to last post

  15. Consent Form advice please

    Started by ldunham, 15th Nov 2017 06:02 PM
    • Replies: 1
    • Views: 110,694
    a123456
    18th Dec 2019, 03:47 PM Go to last post

  16. Delegation log- CVs and GCP certificates

    Started by sab14, 16th Oct 2020 04:11 PM
    • Replies: 1
    • Views: 16,504
    a123456
    18th Jan 2021, 04:22 PM Go to last post

  17. Patient transferring site - Who keeps original trial docs?

    Started by CaraF, 26th Jul 2022 02:54 PM
    • Replies: 1
    • Views: 13,647
    a123456
    31st Jul 2022, 06:18 PM Go to last post

  18. Consent for possible future uses of data

    Started by Catherine, 4th Nov 2011 11:35 AM
    • Replies: 2
    • Views: 8,342
    Rob Wosley
    17th Nov 2011, 06:08 PM Go to last post

  19. Scanned Source Documents

    Started by Jasper, 12th Jan 2012 10:37 PM
    • Replies: 2
    • Views: 11,739
    a123456
    22nd Jun 2012, 05:45 PM Go to last post

  20. Fasting before Consent

    Started by ztarfizh, 26th Nov 2012 11:11 AM
    • Replies: 2
    • Views: 55,779
    a123456
    27th Nov 2012, 03:58 PM Go to last post

  21. GCP certiifcates for local lab staff

    Started by plamb, 10th Jan 2014 01:11 PM
    • Replies: 2
    • Views: 15,041
    plamb
    13th Feb 2014, 12:24 PM Go to last post

  22. Deleted records by site in error

    Started by blsm002, 22nd Sep 2014 06:49 AM
    • Replies: 2
    • Views: 79,230
    Vyara Stefanova
    17th Nov 2014, 08:35 AM Go to last post

  23. Source data queries

    Started by ecsy911, 15th Apr 2015 12:07 PM
    • Replies: 2
    • Views: 32,612
    ecsy911
    28th Apr 2015, 09:08 AM Go to last post

  24. Question Return of consent forms by post (CTIMP in rare disease area)

    Started by CGW1981, 11th Mar 2016 11:18 AM
    • Replies: 2
    • Views: 40,495
    CGW1981
    22nd Mar 2016, 05:13 PM Go to last post

  25. Retrospective Consent for additional samples?

    Started by MsJones, 26th May 2016 10:45 AM
    • Replies: 2
    • Views: 57,362
    MsJones
    1st Jun 2016, 02:33 PM Go to last post

  26. Duration of informed consent after death

    Started by ztarfizh, 31st Jan 2020 01:29 PM
    • Replies: 2
    • Views: 10,225
    a123456
    18th Feb 2020, 08:08 PM Go to last post

  27. SDL Delegated Tasks for Research Nurses

    Started by Leigh, 21st Jul 2016 04:14 PM
    • Replies: 2
    • Views: 40,170
    a123456
    3rd Aug 2016, 12:30 PM Go to last post

  28. Conflict of interest

    Started by debbie.spruce, 13th Feb 2019 11:12 AM
    • Replies: 2
    • Views: 59,266
    debbie.spruce
    18th Feb 2019, 12:14 PM Go to last post

  29. Same person acting as both sponsor AND site staff - inappropriate?

    Started by TrialsAdvice, 16th Feb 2021 07:06 PM
    • Replies: 2
    • Views: 30,852
    a123456
    6th Jun 2021, 03:06 PM Go to last post

  30. Personally dating documents?

    Started by Kar3n, 23rd Mar 2022 01:18 PM
    • Replies: 2
    • Views: 19,143
    a123456
    26th Mar 2022, 08:34 PM Go to last post
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