FALLS CHURCH, Va., Oct. 31 /PRNewswire/ -- The industry's foremost
authorities on clinical research will lead Clinical Trials: Effective
Recruitment and Informed Consent Strategies, a 2 day workshop in
Philadelphia, PA (http://www.fdanews.com/informedconsent), sponsored by the
RxTrials Institute and FDAnews.
This interactive workshop focuses on how to speed the IRB and FDA
review processes, shorten trial cycles and get products to market faster.
For more information on the workshop, call toll free (888) 838-5578, +1
(703) 538-7600 or visit http://www.fdanews.com/informedconsent.
Failure to recruit subjects is the number one reason clinical trials do
not meet deadlines. Compounded by failure to properly consent patients, 72
percent of all trials run over schedule by more than one month and only 6
percent are completed on time. Delayed or canceled studies and negative
publicity can cost companies millions - even billions - of dollars. This
hands-on session will address ways to avoid the industry's biggest
Workshop faculty who will lead this event include:
Christine Pierre, RN, President and CEO, RxTrials, Inc.
Mark Hochhauser, Ph.D., Consultant, Member of the Institutional Review
Board, North Memorial Health Care
Clint Hermes, Partner, Ropes & Gray LLP
Linda Strause, Ph.D., Executive Director, Oncology Clinical Operations,
RxTrials Institute, the foremost expert on clinical research site
management, marketing, and business development, is pleased to present a
comprehensive series of training programs for the clinical research team.
RxTrials Institute is known nationwide for groundbreaking presentations and
customized training programs that are both innovative and dynamic.
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Pharmaceutical and medical device professionals rely on FDAnews' print and
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