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Event Details



An Introduction to Clinical Trials including ICH-GCP

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Who should attend?

Newcomers to the industry, clinical research personnel with up to 2 years experience, those returning to 'the sharp edge' of Clinical Operations, scientists working in related areas.


This highly interactive course with a balance of information, workshops, exercises and quizzes offers a general overview of the drug development process. With this course you will:

- Understand how drugs are developed and learn in brief about the history and business side of drug development
- Find out what rules, guidelines and laws are essential, who the key players and what their responsibilities are
- Learn the top ethical principle and responsibility behind clinical research – protecting the patient
- Become knowledgeable about the safety aspects and how they are handled in clinical research
- Learn about clinical trial methodologies used and the key documents involved
- Know in detail about the activities necessary before the study can start
- Become familiar with the activities performed during and after the conduct of the clinical study


- The Drug Development Process
- Good Clinical Practice / ICH Guidelines / Directives
- 'Who is Who' in Clinical Research – Roles and Responsibilities
- Conducting Clinical Trials: pre-, during and post study activities
- Clinical Trial Methodology and Design
- Understanding and Handling of Adverse Events
- Monitoring Clinical Studies


Early Bird Fee: CHF 1305.00 + 7.7% VAT (valid until: 18.10.2018) Regular Fee: CHF 1450.00 + 7.7% VAT (valid after: 18.10.2018) Group discounts available, please contact for more information. Registration fees include: Course documentation, refreshment, lunch and a course participation certificate.


Tamara Kohler

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