Advanced Good Clinical Practice (GPC) and Clinical Research Course
This 4 hour webinar session is scheduled at the customer's convenience. We recommend two 2 hour sessions but can accommodate different schedules. Please call 585-381-1350 x246 to schedule.
This course is for clinical research professionals and others that have several years’ experience in the conduct of Clinical Trials and want to update their knowledge with the latest GCP changes or discuss more extensive issues in Clinical Research. This course will be updated frequently to ensure it provides the latest knowledge on GCP requirements. The topics listed below are general topics included in the advanced review. The Agenda will be modified and updated as new GCP requirements are instituted by FDA, ICH, and others.
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.
Call for our competitive pricing. Volume pricing and subscription pricing available.
Contact us at 585-381-1350 x246.