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
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