Vivante GMP Solutions Announces Expansion of Technical Staff

July 08, 2010 (PRLEAP.COM) Business News
HOUSTON, Texas July 8, 2010 Vivante GMP Solutions, Inc. ("Vivante"; www.vivante-gmp.com) today announced that it has increased its technical staff in order to assist the Company in its continued growth as a leader in the virus-based biologics contract manufacturing space. Additional staff has been added in the areas of Manufacturing, Quality Assurance, and Quality Control.

"We are very pleased to welcome these new members to the Vivante team," said David Enloe, Vivante's founder, President and CEO. "We are expanding the Vivante team to support increased demand observed in the first six months of 2010. Growth in this sector is strong and we anticipate expanding the team even further by the end of the year to keep up with demand. One of our strengths is our team's broad scientific and technical expertise, and each of the new Vivante personnel, in bringing their own unique combination of experiences and knowledge to Vivante, broadens that expertise even further. As we increase the number of projects we are performing, our enhanced organization will allow us to continue to provide the excellent service our clients are used to receiving."

ABOUT VIVANTE GMP SOLUTIONS, INC.
Vivante provides its clients with flexible, disposable, scalable Good Manufacturing Practices (GMP) production capabilities, including the skills needed to convert early stage, lab-grade production into robust and scalable therapeutic product classes, suitable for clinical studies and commercial use. Vivante offers its clients access to its intellectual property portfolio, which includes patents, proprietary quality and validation systems, and broad GMP knowledge systems. Vivante operates a state-of-the-art GMP clean room facility which includes production and fill/finish capabilities, as well as facilities for research and development and Quality Control. In addition to its GMP manufacturing service, Vivante offers process development and optimization, Quality Control analytical testing, and on- and off-site GMP product storage and distribution to clinical trial sites.