Clinical Conductor CTMS Offers Free GCP Webinar with PEER Consulting Group on October 29th

ROCHESTER, N.Y. - Oct. 10, 2014 - PRLog -- “Insights to Overcome Common GCP Challenges - From Consent to Documentation to Reporting”

October 29th at 3PM ET

Presenter: George Gasparis - President, the PEER Consulting Group

REGISTER NOW: https://www.gotomeeting.com/register/978729410

About This Free Webinar:

In today’s highly regulated environment, researchers sometimes struggle with the amount of requirements governing biomedical research.   With additional policies from institutions and/or sponsors, researchers often feel overwhelmed with regulatory burden.  In this free webinar, you can gain insights on how you can conduct your clinical research in compliance with Good Clinical Practice (GCP) and federal regulations.  This webinar is hosted by George Gasparis, a 33 year veteran in clinical research and research administration.  He will provide tips from years of experience that will help you ensure that you:

- Obtain legally-effective consent from subjects
- Minimize protocol deviations and protocol violations
- Obtain and maintain appropriate documentation of study findings
- Appropriately identify, document, and report adverse events and toxicities
- Manage the investigational product(s) and maintain adequate records

About George Gasparis

George Gasparis has over 30 years of experience in the administration or conduct of human subjects research. Prior to starting “PEER”, he served as the Executive Director, HRPP/IRB at Columbia University (CU), CU Medical Center (CUMC) from 2003-12.  He worked at the Office for Human Research Protections (OHRP) for seven years and served as the Director, Division of Assurances and Quality Improvement from 2000-03, where he led the development of the OHRP QI Program.  He has also served as the Director, GWUMC IRB and as a Data Manager for over 40 clinical trials at GWUMC.