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Basics 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).

Details

The course offers a general overview of the drug development process and most relevant tasks and responsibilities within the clinical research setting

It provides details on how drugs are developed and who the key players in the process are, about the terminology used in the clinical research environment and what rules, guidelines and laws are essential.

How a clinical study is set up and performed and how to handle the documentation required in clinical research.

Prices

Early Bird Fee: CHF 990.00 + 7.7% VAT (valid until: 20.02.2019) Regular Fee: CHF 1'100.00 + 7.7% VAT (valid after: 20.02.2019) 10 % reduction for CTC employees, SwAPP and SBA members. The fee includes course documentation, refreshments, lunch and a course participation certificate. Payment: After registration you will receive confirmation and an invoice with instructions on how to complete the bank transfer. Full prepayment is needed prior to the course. For special fees or group discount, please contact training@ctcresourcing.com

Contact

Tamara Kohler
tamara.kohler@ctcresourcing.com

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