The understanding of the basic elements and key milestones of the Clinical Development of new medicines can help create valuable connections to the publication planning process. Critical information on the progress and results along the pathway from molecule-to-medicine can play an important role in achieving goals across a broad audience spectrum.

This webinar will focus on key aspects of regulations, as well as strategies, elements of research, and clinical trial considerations. Opportunities for publications tied to critical points in the process will be discussed. This event is ideal for investors, prescribers, care-givers, 3^rd-party payers, patients, internal staff, policymakers, and others for whom timely and accurate information may shape decision-making and outcomes.

Panelists:
Karen Bannick, M.A., Principal, BANNICK CONSULTING LLC
Cindy Dempsey, RN, MPH, Medical Writer, MDS PHARMA SERVICES
Sachin S. Devi, Ph.D., Director, Laboratory of Experimental and Clinical Toxicology, Assistant Professor of Pharmacology, School of Pharmacy, LAKE ERIE COLLEGE OF OSTEOPATHIC MEDICINE
Elisabeth M. Fine, PhD, CMPP, Manager, Publications, MILLENNIUM, THE TAKEDA ONCOLOGY COMPANY, GLOBAL MEDICAL AFFAIRS

Moderator:
Elizabeth vonRentzell, Clinical Research Associate, CROSSTREES MEDICAL

Register Today!

Individual Registration - $395
Any subsequent registrations will receive a 15% discount.

*Group Registration Options - $1,995
Access for 45 or fewer attendees from the same company. For group registrations of 45 or more, please contact Kathie Eberhard at 704-341-2439 or keberhard@frallc.com.

*Please note when registering delegates under Group Registrations you must submit an advance list of attendees from your organization including email address and name.