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ICH GCP Refresher

Inspections, current issues and hot topics

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Who should attend?

Designed for those with experience in clinical research seeking to update their knowledge on the changes to the ICH-GCP Guideline E6 R2 and for those requiring information on how to prepare for GCP inspections. It is aimed at Clinical Research Assistants/Coordinators, Clinical Trial/Project Managers, Clinical Research Physicians, Study Data Managers, Monitors, those working in Clinical Quality and Compliance, and will also be of interest to those in related functions (Clinical Science, Drug Supply, Drug Safety, Regulatory).

Details

This course offers a thorough update of the current understanding and interpretation of Good Clinical Practice and practical guidance/advice on how to ensure readiness for Health Authority inspections, both of Sponsor and Investigator sites.

Prices

Early Bird Fee: CHF 990.00 + 7.7% VAT* (valid until: 12.09.2019) Regular Fee: CHF 1'110.00 + 7.7% VAT* (valid after: 12.09.2019) 10 % reduction for CTC employees, SwAPP and SBA members Registration fees include: Course documentation, refreshments, lunch and a course participation certificate. For special fees and group discounts, please contact: training@ctcresourcing.com

Contact

Tamara Kohler
tamara.kohler@ctcresourcing.com

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