Philadelphia, PA (PRWEB) January 22, 2013
ERT, a global technology-driven provider of health outcomes research services to biopharmaceutical organizations, medical device companies and contract research organizations (CROs), today announced a series of upcoming industry conferences and company-sponsored events which will feature presentations by members of ERT’s scientific and regulatory teams.
Scientific and regulatory experts from ERT will share their knowledge on the collection of high-quality patient safety and efficacy data at the following events:
For additional information on these events and other opportunities to meet with the ERT scientific and regulatory team, please visit http://www.ert.com/news-events.
ERT (http://www.ert.com) is a global technology-driven provider of health outcomes research solutions and services supporting biopharmaceutical and medical device organizations to achieve their new medical product development and commercialization objectives. ERT harnesses leading technology coupled with reliable processes and scientific/regulatory expertise to collect, analyze and report on clinical trial data to support the determination of health outcomes critical to the approval, labeling and reimbursement of pharmaceutical and new medical products. ERT is the acknowledged industry leader in centralized cardiac safety, respiratory efficacy services, scientific and regulatory consulting, and Clinical Outcome Assessment (COA) solutions, which includes patient, clinician, and observer reported outcomes. ERT is a global organization with headquarters in Philadelphia, PA and offices throughout the U.S., U.K., Japan, and Germany.