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Good clinical practice is a set of rules and regulations that is provided by International Conference on Harmonisation - an international body that regulates clinical trials involving human subjects.
Good clinical practice guidelines include protection of human rights as a subject in clinical trial. It also provides assurance of the safety and efficacy of the newly developed compounds.
Good clinical Practice Guidelines includes regulations on how clinical trials should be conducted, define the roles and responsibilities of clinical trial sponsors, clinical research investigators, and Clinical research associates.
External links
- ICH Website
- FDA Website
- Clinical Research Training & GCP Resources
- Free to use online series of GCP Challenge Tests
- Clinical Research Training
- Careers in Clinical Research
- Clinical Research Services
- Clinical Research Companies Listings
- International Clinical Research Services and Corporate Trainings
- PharmaSchool JargonBuster Clinical Trial Terminology Dictionary
- Clinical Research Abbreviations and Acronyms
- Clinical Research Glossary / Definitions
- List of Food and Drugs Regulatory Agencies
- Clinical Research: Frequently asked questions
- WikiProcess - A repository of Best Practices of all areas. Lists of step by step guides of proven processes and methods to achieve a goal.
- Good Clinical Practice: A Question and Answer Reference Guide 2006
"Good clinical practice"