Twice monthly, CWWeekly provides featured listings of clinical research job openings, upcoming industry conferences and educational programs from JobWatch, CenterWatch's online recruitment website for both clinical research employers and professionals.
With ICH E8(R1) set to be adopted in June 2020, your planning, design and conduct of clinical trials will look different than they do today. Make sure you’re ready to implement the new guidelines. This webinar clarifies how.
Webinar Takeaways:
The purpose of the ICH E8 guideline and its relationship to other ICH
Efficacy guidelines, including ICH E6(R2) (Good Clinical Practice [GCP]) and ICH E9 (Statistical Principles for Clinical Trials)
The impact to current research
practices that could influence your SOPs, procedures, processes and
documentation pertaining to ICH guidance
First to market: A coveted spot you aspire to reach in the crowded life sciences arena. You have multiple SOPs in place to improve efficiency and ease of use, in an effort to minimize wasted time and win that sought-after place. But you are far more likely to be first to market when your SOPs and digital solutions are integrated, ensuring nothing falls through the cracks. After all, if you don’t know there’s a problem, you can’t address it.
