Quality Data...Delivered by Design™

Quality Data...Delivered by Design™



Webinar: Monitoring in the 21st Century: What the Investigative Site Needs to Know


Course Title

Monitoring in the 21st Century: What the Investigative Site Needs to Know


Date

This webinar session is scheduled at the customer's convenience. Please call 585-381-1350 x246 to schedule.


Summary

This webinar discusses how FDA’s new draft guidance on Risk-Based Monitoring will affect Investigators and Coordinators’ daily study activities as well as when the monitor is performing monitoring activities.


Key Points

  • Review FDA’s new guidance on monitoring
  • Discuss how it will affect Investigator Sites
  • Learn how Investigator Sites may adjust to new monitoring procedures

Recommended Attendance

  • Investigators
  • Monitors
  • Clinical Research Coordinators
  • Clinical Research Associates/Monitors
  • Project Managers
  • GCP Auditors

Instructor Bio

Lorraine D. Ellis, MS, MBA.
Ms. Ellis is an experienced trainer with in-depth knowledge as a result of hands-on experience in clinical trials and training thousands of clinical research professionals over decades. Ms. Ellis has over 30 years clinical research experience and is the author of several books, articles and other clinical research materials. She has authored and taught over 50 courses designed for clinical research professionals.

She has presented at major industry meetings such as DIA, ACRP, CRO Partnerships and others. Ellis has also served as faculty for ACRP courses, participated in the development of ACRP certification programs, and is an adjunct professor in the MS in Clinical Research Management program at Rochester Institute of Technology.


Cost

$99 per person


To Register

If you are interested in attending/scheduling this webinar, Contact us at 585-381-1350 x246.


For other available webinars or on-site courses

Visit our website's training section or Contact us at 585-381-1350 x246.