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2022 FDA Good Clinical Practice Guide: The One-Stop Resource for Clinical Trial Regulations and Guidelines - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "FDA Guide to Good Clinical Practice" directory has been added to ResearchAndMarkets.com's offering.

This resource is THE most comprehensive and straightforward resource of its kind.

The Guide to Good Clinical Practice is your one-stop resource for clinical trial regulations and guidelines - everything you need to conduct clinical trials more effectively, streamline the process and ensure human subject protection and trial data integrity.

Key Topics Covered:

  • Overview of Good Clinical Practice
  • Investigator Obligations
  • Information About Subjects
  • Document Requirements
  • Sponsor/Monitor Obligations
  • Evaluation of Clinical Data
  • Quality Assurance Audits
  • Institutional Review Boards
  • International Good Clinical Practice
  • Electronic Submissions, Computer Validation
  • FDA Monitoring
  • Other Federal Authorities

For more information about this directory visit https://www.researchandmarkets.com/r/r9vxro

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com

For E.S.T. Office Hours Call 1-917-300-0470
For U.S./ CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

Industry:

Research and Markets

Release Versions
English

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com

For E.S.T. Office Hours Call 1-917-300-0470
For U.S./ CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

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