ICH GCP guideline rewrite - the future is now

A practical orientation course on the revision to ICH GCP as it is being implemented across the industry and academia. This is the largest update to Good Clinical Practice in over 20 years, so even seasoned professionals will benefit in learning from some of the members of the expert working group responsible for writing the document.

The course is designed to give all clinical trials professionals an understanding of the thought processes behind the revision and the expectations in terms of proportionality, risk based quality management, data governance and the use of technology in clinical trials.

The course is given by GCP experts from Regulatory Authorities and industry who truly understand the current clinical trial landscape and use their expertise to look at the application of GCP to various scenarios from trial design to reporting.

Swiss Biotech Members are eligible to a 10% discount on registration fees. Add discount code: SWISSBIO in the cart at the end of your purchase order.