NSF GMP Registration Compliance 4/1/2019
NSF GMP Registration Compliance
Salt Lake City, Utah (January 4, 2019) 4Life’s Sandy and Vineyard manufacturing facilities have received NSF® International’s Good Manufacturing Practice (GMP) Registration for 2019.

Earning GMP Registration from NSF International verifies that 4Life uses the proper methods, equipment, facilities, and controls for producing dietary supplement products.

Senior Director of Quality Adam Briggs: “We are committed to providing the highest quality products for our customers and distributors alike. Earning NSF GMP Registration shows our investment and distinguishes our products with greater credibility.”

GMP guidelines help companies develop and maintain proper controls in their manufacturing process so that products are processed, manufactured, and labeled in a consistent manner, as well meet quality standards. The NSF GMPs were developed in accordance with the U.S. Food and Drug Administration’s (FDA) regulations on dietary supplement manufacturing, packaging, and distribution.

Chief Scientific Officer David Vollmer, PhD: “Our manufacturing facilities give us complete control over batching, blending, encapsulating, and packaging of primary 4Life Transfer Factor Products. The NSF GMP Registration provides a well-known, third-party endorsement for our commitment to overall quality.”

4Life has offices in 25 markets to serve a global network of independent distributors and their customers.

For more information:
Calvin Jolley
Vice President
Corporate Communications
4Life Research USA, LLC
[email protected]