LAWRENCEVILLE, New Jersey – Oct. 10, 2019 – Xybion Corporation, a US-based leading global technology provider for companies operating in the highly regulated industries, announced today that U.S. Food and Drug Administration’s (FDA) National Center for Toxicological Research (NCTR) awarded a multi-year contract to Xybion. After a competitive RFP process titled COTS “Pre-Clinical Data Management System” Software. NCTR selected Xybion’s Pristima XD for various toxicology functions and Savante for producing CDISC SEND format data to replace the organization’s existing data management system with a modern, integrated, and comprehensive solution.
Xybion’s Pristima XD and Savante were selected through FDA’s competitive sourcing program amongst multiple vendor proposals and the award includes licensing, implementation, and validation services, utilizing Xybion’s expert staff to install, train and validate the Pristima Suite at NCTR. Dr. Pradip K. Banerjee, Chairman and CEO of Xybion said “We are delighted to have the privilege of working with FDA’s NCTR division to support its mission of promoting and protecting the public health of our country.” Dr. Banerjee further stated “This is an important win for Xybion, strengthening our commitment to support and improve research and development in the Federal Government. Xybion provides high-quality, transformational services and solutions to help our customers solve their most complex challenges.”
Scope of the awarded contract includes:
“We are thrilled to partner with the FDA and welcome its scientific team to the Xybion Pristima XD community. We are excited to deliver industry-leading study management, informatics, and analytics solution to NCTR to facilitate and expedite the research of innovative new products and medicines” stated Kamal Biswas, Xybion’s President, and COO.
Xybion is a leading software, services, and consulting company dedicated to helping corporations solve business problems.
Through intelligently designed systems and business processes, we help companies become more efficient, reduce costs, and manage compliance, regulatory adherence, and risk. Serving more than 160 customers in 25 countries. Xybion has the global scale and expertise to bring employees around the world together to manage complex business processes and improve program administration.
Xybion business segments include life sciences, workplace health, manufacturing, government, and enterprise solutions.
We put our expertise into action every day to help companies transform the digital workplace. Our unique solutions focus on regulatory compliance, GRC, quality management, GLP, integrated preclinical lab management, early-stage drug discovery, content migration, and systems validation. Since its founding in 1977, Xybion Corporation has supported, through software, services, and consulting top 20 global life sciences companies.
Head of Quality Assurance
Heidi leads Xybion’s Quality Assurance practice. She has over 20 years’ experience in designing and implementing quality assurance policies. Since joining Xybion in 2000, Heidi worked with several clients to design quality policies and ensure compliance. She is responsible to hosting Xybion customer audits. Heidi has a BA degree in Biology from The King’s College.