Essential Documentation within Clinical Research
Essential Documentation within Clinical Research
Video: .mp4 (1280x720, 30 fps(r)) | Audio: aac, 44100 Hz, 2ch | Size: 226 MB
Genre: eLearning Video | Duration: 6 lectures (33 mins) | Language: English
An introductory course into Essential Documents required for the conduct of a clinical trial
Video: .mp4 (1280x720, 30 fps(r)) | Audio: aac, 44100 Hz, 2ch | Size: 226 MB
Genre: eLearning Video | Duration: 6 lectures (33 mins) | Language: English
An introductory course into Essential Documents required for the conduct of a clinical trial
What you'll learn
This course will look at the purpose of Essential Documents. These documents serve to demonstrate the compliance of the investigator, sponsor and monitor with the standards of GCP and with all applicable regulatory requirements.
Requirements
This course is for anyone woking with clinical research or with a keen interest.
Description
This comprehensive course for Essential Documents will give you all the required information you need regarding documentation required for the conduct of a clinical trial. This course will cover
•Define Essential Documents and their purpose
•Understand what ICH GCP E6 R2 says about Essential Documents
•Investigate eTMF systems and their place in accurate storage and retrieval of Essential Documents
•Understand how to archive Essential Documents according to ICH GCP standards
Who this course is for:
This course is for anyone woking with clinical research or with a keen interest.
Essential Documentation within Clinical Research
