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Event Details


From Molecule to Medicines - An Introduction to Clinical Trials including ICH-GCP

From Molecule to Medicines - 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

Course Topics

  • The Drug Development Process
  • Good Clinical Practice / ICH Guidelines / Directives
  • “Who’s 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 1'305.00 + 7.7% VAT (valid until: 25.01.2018) Regular Fee: CHF 1'450.00 + 7.7% VAT (valid after: 25.01.2018) Please contact us for special group registration offer


Training Department

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