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Event Details


Basic Course in Clinical Research

Basic Course in Clinical Research

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Who should attend?

This course is designed for those with little or no experience in clinical research or those seeking an overview of the clinical research process, regulations, terminology, acronyms, roles and responsibilities within clinical research. It is aimed at Clinical Research Assistants, support staff and persons with related functions (eg. IT Support Staff).


The course offers a general overview of the drug development process and most relevant tasks and responsibilities within the clinical research setting, focusing on practical aspects and mainly addressing the needs of assistants and support personnel. With this course you will:

  • Understand how drugs are developed and who the key players are in the process
  • Become knowledgeable about the terminology used in the clinical research environment
  • Find out what rules, guidelines and laws are essential
  • Learn how a clinical study is set up and performed
  • Become familiar with and understand how to handle the documentation required in clinical research


  • Developing a drug in the pharmaceutical industry – from the idea to the product you buy in the pharmacy – and the contributions of clinical research
  • What is a clinical study – the four phases of clinical development
  • Who are the key players and what are their roles in the process
  • The language and abbreviations the clinical research team are using every day
  • What are the rules, guidelines and laws that need to be followed and why are they so important
  • How is a clinical study performed – from preparation over conduct to termination of a study
  • A key to a successful study: the master study file. What documents are essential and how are they handled, filed and archived?


Early Bird Fee: CHF 855.00+ 7.7% VAT (valid until: 02.03.2018) Regular Fee: CHF 950.00 + 7.7% VAT (valid after: 02.03.2018) Please contact us for special group registration offer


Training Department

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