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ERT Reaches Milestone in Supporting Successful New Drug Approvals
Date:1/8/2014

sk in preparation for regulatory inspections of ePRO data collection systems. The paper is available for complimentary download at http://www.ert.com/clinical/resources/white-papers/.

For additional information on ERT’s proven cardiac safety, respiratory, and eCOA products and services, visit http://www.ert.com/clinical/clinical-endpoints/.

About ERT

ERT (http://www.ert.com) is a leading provider of high-quality patient safety and efficacy endpoint data collection solutions for use in clinical drug development. ERT delivers a combination of technology, services, and consulting that increase the accuracy and reliability of patient data and improve the efficiency of the clinical development process throughout the product lifecycle. ERT delivers the most widely deployed solutions in centralized cardiac safety, respiratory services, suicide risk assessment and Clinical Outcome Assessments (COA) – which includes patient, clinician, and observer reported outcomes. By efficiently integrating these solutions through a system built upon a scientific and regulatory foundation, ERT collects, analyzes, and delivers safety and efficacy data critical to the approval, labeling, and reimbursement of pharmaceutical products. ERT is a global organization with headquarters in Philadelphia, PA and offices throughout the U.S., U.K., Japan, and Germany.

Read the full story at http://www.prweb.com/releases/2014/01/prweb11470975.htm.


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