CINCINNATI, June 9 /PRNewswire/ -- Medpace, Inc. ( http://www.medpace.com/ ), a full-service contract research organization, announced the opening of their 35,000 square foot laboratory located at their new headquarters in Cincinnati, Ohio. Medpace moved to the new facility in December, 2003.
"Medpace Laboratories is an extension of the contract research offerings that Medpace has provided since 1992," said Debbie Bruce, Manager of the Medpace Laboratories. "The laboratory includes new state-of-the-art, high through-put instrumentation and long-term sample storage units." Preparation, packaging, and delivery of all supplies and materials necessary for specimen collection are managed within the laboratory.
ClinTrak(R), a comprehensive proprietary software system, designed to organize the management of clinical trials, will be used to collect and analyze clinical trial data. Study-specific information generated by the laboratory is integrated into ClinTrak, facilitating a seamless transfer of data between collaborating study personnel. Customized status reports and other unique reporting requirements are made available throughout the course of a project. Secure, web-based reporting is provided, which is readily accessible by Sponsors and investigational sites.
"The goal of Medpace Laboratories is to provide the highest quality analytical support to Sponsors and investigational sites. The laboratory offers a comprehensive test menu, from routine chemistries to molecular diagnostics," said Dr. August Troendle, President and CEO of Medpace. "We are very pleased to offer this service to our valued customers."
Medpace Laboratories is compliant with the Clinical Laboratory Improvement Amendment (CLIA-88) and accredited by the College of American Pathologists (CAP). The laboratory employs medical technologists that are certified by the American Society for Clinical Pathology (ASCP).
About Medpace
Established in 1992, Medpace has partnered with leading pharmaceutical companies to bring promising new drugs to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide Sponsors with exceptional support during the drug development process.
The integrated services at Medpace include: clinical development plan preparation, study management, central laboratory services, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and US and international regulatory submissions.
Media Contact: Sally Dressman 513-579-9911
Medpace, Inc.CONTACT: Media, Sally Dressman of Medpace, Inc., +1-513-579-9911
Web site: http://www.medpace.com/
