LAWRENCEVILLE, N.J. (PRWEB) JANUARY 08, 2018- Xybion Corporation, a US-based global technology solutions provider for companies operating in the highly regulated industries, announced today that Level Biotechnology Inc., a leading Taiwan-based biotechnology company, has signed a software subscription agreement for Pristima XD, Xybion’s flagship preclinical solution and Savante, its popular module for the production of FDA compliant SEND submissions.
This agreement follows an extensive analysis of all competitors in the preclinical space and allows Level Biotechnology Inc. to leverage Pristima’s core components, such as Clinical Pathology, Animal Room, Necropsy Room, and Histopathology to support its preclinical laboratory services.
Xybion will be providing Pristima XD Software-as-a-Service (SaaS) solution, utilizing hosted (private cloud) services from its Singapore data center. Importantly, Pristima XD will be interfaced to support real-time communications with clinical pathology instruments at Level Biotechnology. “Level Biotechnology was looking for a comprehensive integrated SaaS solution, which would help us push compliance across our business functions and allow us to optimize our preclinical operations,” stated Emerson Chiu, President of Level Biotechnology. “We went through a rigorous search for the best solution, and we felt that Xybion’s partnership and their industry-leading Pristima XD software platform is the right fit for our organization.”
Expressing confidence in this partnership, Carlos Frade, Vice President of Preclinical R&D Solutions at Xybion said, “We are excited about being selected by Level Biotechnology for our preclinical suite. I am confident in Xybion’s decades of expertise in the preclinical market and certain that deployment of our Pristima XD and Savante solutions will immediately benefit Level Biotechnology’s efficiency, productivity, and reporting timelines.”
Xybion’s Chief Executive Officer, Dr. Pradip Banerjee went on to say “At Xybion, we strive to earn the trust and support of our clients and create a lasting position of a valued partner.” Dr. Banerjee continued, “We see Xybion’s footprint and reputation expanding globally and seek to set an industry benchmark in the APAC market. We look forward to a long-term business relationship with Level Biotechnology.”
About Xybion Corporation
Xybion is the leading provider of software, services, and consulting for global corporations operating in highly regulated industries. Our unique solutions focus on regulatory compliance, GRC, quality management, GLP, integrated preclinical lab management, early-stage drug discovery, content migration, and systems validation. Xybion specializes in helping companies improve their overall compliance processes and provides a complete view of organizational risk across global organizational models.
Xybion’s combination of software, business process management, services, validation, and staffing enable us to cover a broad spectrum of critical business needs for companies and we deliver our solutions on a global scale. Since its founding in 1977, Xybion Corporation has supported, through software, services, and consulting, 100% of the top 20 global life sciences companies. Our leadership in this dynamic and ever-changing industry has been a cornerstone of our high-value reputation.
About Level Biotechnology Inc.,
Founded in 1989, Level Biotechnology Inc. has been providing the best preclinical CRO services and end-to-end solutions for biomedical research and drug development in Taiwan. Its CRO services support more than 9,900 square yards of laboratory space.
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.