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 Essential Documentation within Clinical Research

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MensajeTema: Essential Documentation within Clinical Research   Essential Documentation within Clinical  Research EmptySáb Mayo 16, 2020 4:55 pm

Essential Documentation within Clinical  Research Cc95142a5453cdac3af0ec364a649b9b
MP4 | Video: h264, 1280x720 | Audio: AAC, 44.1 KHz, 2 Ch
Genre: eLearning | Language: English + .srt | Duration: 6 lectures (32m 36s) | Size: 140.4 MB
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.

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Essential Documentation within Clinical  Research 0861318949f53e26d16462a9e6e5561c

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