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Sponsors and CROs are under increasing pressure to monitor and manage risk from various perspectives and under multiple FDA guidances. Complying with regulations such as ICH E6(R2), while meeting milestones and addressing issues, is time-consuming and costly.
TORONTO (PRWEB) January 07, 2019
Join industry experts Julie Peacock, Client Services at Comprehend and Heather Davis, Independent Consultant at Maven Ridge for a live webinar on Thursday, January 17, 2019 at 1pm EST.
This webinar will dive into best practices for the identification and ongoing management of risk during the clinical trial process. Featured speakers will also present a case study of a leading pharmaceutical company that faced multiple challenges affecting its risk profile.
Best practices will be discussed during the presentation—including how to define, analyze, and operationalize the risk management process in the study conduct phase—that you can use to answer important questions, such as:
Join Heather Davis, an industry veteran with more than 26 years of experience in clinical trials, and Comprehend for this informative webinar.
For more information or to register for this event, visit Collaborative Risk Management: Plan & Pivot Your Clinical Studies.
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
For the original version on PRWeb visit: https://www.prweb.com/releases/collaborative_risk_management_plan_pivot_your_clinical_studies_new_webinar_hosted_by_xtalks/prweb16015624.htmNEXT ARTICLE
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