Introduction to Clinical Research
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This course explains the key stages and phases of the drug development process and is a perfect opportunity to quiz industry experts on who does what and why.

What Is The Course About?
This course will provide you with a complete overview of the clinical research process and provides a good understanding of the drug development industry. It is particularly relevant to people who have less than 2 years experience of the industry or are working in a support role.

By the end of this course, you will be able to:
- Understand the key stages and phases of drug discovery and clinical research.
- Understand how regulatory authorities interact with drug development companies.
- Understand the importance of ethics, safety and efficacy in clinical research.
- Understand the importance of the role of the CRA.
- Understand the importance of clean data and the role of the data management team.
- Understand how the trial is designed and the impact of the statisticians at this point.
- Understand the principles of good project management practice.

The full fee for this course is £1,590 +vat and includes full course materials, lunch and refreshments.

Course Programme:
Introduction To Clinical Research
DAY ONE
Introduction & Objectives
Overview of Drug Development
Regulatory Affairs - An Overview
ICH & GCP
Clinical Trial & Protocol Design
CRF Design
Clinical Report Writing & Publications

DAY TWO
Protection of the Subject in Clinical Research
GCP Inspections and Audits
The Role of the CRA
Recruitment of Investigators
Monitoring The Study

DAY THREE
Introduction to Data Management
Introduction to Statistics
Project Management of Clinical Trials
 
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The course either has new dates in data loading, or is only run as a dedicated or In Company course.
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Key Details
Duration3 days
 
£1,590
per delegate
 
 
Bookings Helpline: 01933 233884 (Monday to Thursday - 8:00am to 5:30pm and Friday 8:00am to 5:00pm).