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An Introduction to Clinical Trials and Drug Development
Course Summary
This module provides an understanding of how clinical trials fit into the drug development process. It outlines the key historical events leading to the development of controlled clinical trials. It specifies the purpose of trials, outlines their features, and identifies codes and regulations that apply to them. Finally, it describes the environment of cost control in which the modern pharmaceutical industry operates.
Purchasing Information
When you have completed your course order, Zenosis will finalise the setup of your course materials and contact you on the email address that you provide in your order. You can expect this process to be completed within one business day (using the UK business calendar) of completing your payment.
It is therefore essential that you use your real email address for your order, or indicate in the purchase notes the email address to be used for the course set-up, and check that any messages from Zenosis or grapl are not lost in your junk or spam folder.
You will have access to the course module(s) for a period of 180 days after your purchase is complete.
Detailed Course Information
Learning Objectives
• Describe the key events in the historical development of the modern pharmaceutical industry.
• Outline the key codes of practice and regulatory processes.
• Explain how clinical trials fit within the drug development process.
• Describe the economic environment within which pharmaceutical companies operate.
Who will benefit from this course
This introductory module is an ideal primer for those new to the fields of clinical research or regulatory affairs. It will also provide valuable background information for administrative, sales and other staff in the pharmaceutical and biotechnology industries, enabling them to understand better the context in which they work.
Module Outline
• Overview
– The context of the pharmaceutical industry and modern medicine is established. The module’s four perspectives on clinical trials are setout.
• History
– Factors that gave rise to the modern framework of regulation of clinical trials are traced.
• Codes and regulations
– The principal elements of regulation of clinical trials are set out. The regulatory frameworks of the USA, Europe and Japan are outlined. International harmonisation of requirements through the work of ICH is discussed, with particular reference to Good Clinical Practice.
• Drug development
– The long and financially risky process of developing a drug is described. The various stages of discovery, nonclinical and clinical development are detailed.
• Global market
– Commercial considerations in drug development are described. Issues such as financial risk, pharmacoeconomics, patent life and generics are discussed.
• Assessment
– Multiple-choice mastery assessment.
Roles
Research, Regulatory, Compliance, Other
CPD Points
1.5
Region
Level
Foundation
Course Study Time
Approx 1.5 hours
USA, Europe, Other