SALT LAKE CITY, UT--(Marketwired - December 01, 2015) - Today, 4Life General Managers from around the world gathered for a ribbon-cutting at the new 4Life manufacturing facility in Vineyard, Utah.
The facility will adhere to current Good Manufacturing Practices (cGMP) as outlined by the Food and Drug Administration (FDA) and includes state-of-the-art packaging, encapsulation, and blending equipment to ensure the highest level of product quality.
4Life broke ground on the new manufacturing facility in December 2014 in order to meet the needs of its expanding global business.
President & CEO Steve Tew: "The completion of this facility gives us start-to-finish control over every step of the manufacturing process, including the batching, blending, encapsulation, and packaging of most 4Life Transfer Factor® products."
Raw materials and finished goods will continue to be tested by 4Life scientists in the company's analytical laboratory. The new facility will include manufacturing of 4Life® Transfer Factor Plus® Tri-Factor® Formula, 4Life Transfer Factor® Tri-Factor® Formula, and Renuvo®.
"As an industry leader in the science of supplementation, our new manufacturing facility will guarantee quality and customer satisfaction for years to come," said Founder David Lisonbee from Brazil.
For more photos of the facility, ribbon-cutting highlights, and the activity of worldwide general managers, visit the 4Life Research® Facebook page. 4Life has offices on five continents to serve a global network of independent distributors through science, success, and service.
Image Available: http://www.marketwire.com/library/MwGo/2015/12/1/11G074199/Images/4life_image1-42a8ff89ecc49954bd6d5c4e96c07ca8.jpg
Contact Information:
For more information:
Calvin Jolley
Vice President, Communications
4Life Research USA, LLC
CalvinJolley@4life.com
