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Overview| Course Title: Overview of Clinical Trials | This course is designed to provide a clear understanding of clinical trial processes and phases for anyone wanting an insight into clinical trials - including those working in clinical research or who work with clinical research professionals.
This detailed programme will provide an insightful understanding of the specific clinical research issues and processes used in clinical research, from Phase I to gaining regulatory approval. Delegates will examine the processes and key functions used within clinical trials including working to the Clinical Trial Directive and GCP Directive. The jargon and terminology frequently used in clinical research will be explained and demystified. Participants will gain a clear understanding of international clinical trials so that they will work more effectively with clinical research professionals.
By the end of the course, you will be able to:
- understand the phases of clinical research and how they advance a drug to market globally
- become familiar with the terminology and the key tools of clinical research
- understand the roles of the key people involved in clinical trials
- gain a step by step guide to how clinical trials are set up and run globally
- appreciate the special considerations for running clinical trials internationally
- understand how data from clinical trials is managed
- become aware of the regulatory control of international clinical trials
- become familiar with the requirements of the Clinical Trial Directive and GCP Directive on running clinical trials
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Available Dates |
Contacts| Name | Telephone | Email |
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| Mrs Anne-Marie Dykes | +44 (0)118 384 2040 | ad@rostrumtrainingsolutions.com |
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Course Literature
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