Udemy - Good Clinical Practice Refresher For Investigators

  • CategoryOther
  • TypeTutorials
  • LanguageEnglish
  • Total size1003.6 MB
  • Uploaded Byfreecoursewb
  • Downloads11
  • Last checkedMar. 22nd '26
  • Date uploadedMar. 21st '26
  • Seeders 4
  • Leechers8

Infohash : 11181E7CE25E6513D27806383DA9DA82614EAB33

Good Clinical Practice Refresher For Investigators

https://WebToolTip.com

MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 1003.59 MB | Duration: 1h 34m

Complete, Certified ICH GCP E6 (R3) Course for Investigators and Site Personnel

What you'll learn
Identify and understand the ICH-GCP requirements throughout the conduct of clinical trials
Learn the core principles of ICH-GCP R3 and how to implement them in practice
Define the roles and responsibilities of each involved key stakeholder: Ethics Committees, Sponsors and Investigators
Understand the purpose of the essential documents and the best practice for filing in the TMF
Understand the essential requirements and contents of the Investigator's Brochure and the Protocol
Practice on real cases: Identify common ICH-GCP inspection findings (FDA warning letters) and how to avoid them
Practice on real cases: Conduct a gap analysis in your organization based on a real MHRA inspection report

Requirements
No prior working experience or knowledge in clinical research is required to attend this course
This course is dedicated to beginners as wells as to more advanced professionals willing to refresh their knowledge

Files:

[ WebToolTip.com ] Udemy - Good Clinical Practice Refresher For Investigators
  • Get Bonus Downloads Here.url (0.2 KB)
    • ~Get Your Files Here ! 1 - Principles Of Ichgcp R3
    • 1 - Why Principles.mp4 (52.4 MB)
    • 2 - The 11 Principles Of Ich Gcp E6 R3 And Practical Advices.mp4 (622.0 MB)
    2 - Responsibilities Of The Investigator
    • 1 - Investigators Responsibilities.html (0.0 KB)
    • 10 - Informed Consent Of Trial Participants.mp4 (80.5 MB)
    • 11 - End Of Participation In A Clinical Trial.mp4 (24.2 MB)
    • 12 - Investigational Product Management.mp4 (20.5 MB)
    • 13 - Randomisation Procedures And Unblinding.mp4 (6.5 MB)
    • 14 - Informed-consent-checklist.pdf (42.7 KB)
    • 14 - Records And Reports.mp4 (56.3 MB)
    • 3 - Qualifications And Training.mp4 (7.3 MB)
    • 4 - Resources.mp4 (10.3 MB)
    • 5 - Responsibilities.mp4 (31.6 MB)
    • 6 - Communication With Irb Iec.mp4 (9.9 MB)
    • 7 - Compliance With Protocol.mp4 (10.1 MB)
    • 8 - Premature Termination Or Suspension Of A Trial.mp4 (27.4 MB)
    • 9 - Participant Medical Care And Safety Reporting.mp4 (44.5 MB)
    • Bonus Resources.txt (0.1 KB)

Code:

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