Udemy - Ich-Gcp - Good Clinical Practice(Quiz + Guideline + Extra Lecture

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Udemy - Ich-Gcp - Good Clinical Practice(Quiz + Guideline + Extra Lecture (Size: 2.1 GB)
  1 - Institutional Review BoardIPR.html 0 B
  1 - Introduction.mp4 42.2 MB
  10 - ICH GCP Preview.mp4 17.1 MB
  11 - ICHGCP Principles Importance Link.mp4 213.2 MB
  12 - ICH GCP E6 R2 Guidelines.mp4 52.5 MB
  13 - Clause 21213.mp4 130.6 MB
  14 - Investigator Clause 4143.mp4 61.5 MB
  15 - Clause 4447.mp4 32.1 MB
  16 - Clause 48413.mp4 56.3 MB
  17 - Sponsor Clause 50510.mp4 140.5 MB
  18 - Sponsor Clause 511523.mp4 85.5 MB
  19 - Quality Module 32 P2.mp4 43.1 MB
  2 - Pharma Regulatory Jargons.mp4 211.6 MB
  2 - Question.html 102.4 B
  3 - DMF.mp4 130.9 MB
  3 - Multiple Choice Type Questions.html 102.4 B
  4 - Audit.mp4 95.1 MB
  5 - Regulatory Compliance and Requirements.mp4 141.3 MB
  6 - Regulatory Regime India US and EU.mp4 141.6 MB
  7 - IPR Copyrights and Patents.mp4 314.2 MB
  8 - IPR in India.mp4 127.9 MB
  9 - IRB or IEC.mp4 88.8 MB
  Bonus Resources.txt 409.6 B
  Get Bonus Downloads Here.url 204.8 B
  ▲ 24 total files

Description


Ich-Gcp:Good Clinical Practice(Quiz+Guideline+Extra Lecture
https://DevCourseWeb.com

Published 8/2023
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz
Language: English | Size: 2.08 GB | Duration: 1h 59m

Unlocking ICH-GCP E6 R2: A Complete Guide to Good Clinical Practice in Clinical Research

What you'll learn
In the ICH GCP (International Council for Harmonisation - Good Clinical Practice) course, students will learn the essential principles and guidelines
for conducting clinical trials ethically and ensuring the safety and well-being of human participants.
They will gain a comprehensive understanding of the regulatory requirements, documentation, and standard operating procedures involved in the entire clinical tr
The course will cover topics like trial design, informed consent, data collection, monitoring, adverse event reporting, and quality assurance.
By completing the course, students will be equipped with the knowledge and skills necessary to adhere to GCP standards
contribute to successful and compliant clinical research.

Requirements
Clinical Research Organizations staff, students
Beginners

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