Salt Lake City, UT (July 10, 2024) Since 2017, 4Life
® manufacturing facilities have been NSF certified. Most recently, the company passed an audit with an “A” grade. Additionally, 4Life
® Transfer Factor Plus
® Tri-Factor
® Formula received continued
contents accreditation from NSF by passing the annual audit required to maintain that certification.
In the United States, dietary supplement manufacturing facilities must be registered with the Food and Drug Administration (FDA) as food processing facilities. 4Life manufacturing facilities are held to the standards of U.S. Code Title 21 Part 111, which prescribes current Good Manufacturing Practices (cGMP).
Senior Vice President, Quality, Steve Pederson: “The auditor repeatedly complimented the superior condition of our facilities and called out the cohesiveness of our operations and positivity of our team members. Special thanks to Director of Quality Assurance, Jim Dimmick, as well to each process owner in our Global Supply Chain department. An A audit doesn’t happen overnight. The grade is the result of the highest level of professionalism in Manufacturing, Distribution, Purchasing & Planning, Quality, Human Resources, and Research and Development.”
NSF International is an independent third-party certifying organization that audits procedures, programs, facilities and equipment, documentation practices, grounds, sanitation, laboratory operations, and product contents to ensure quality and Good Manufacturing Practices.
4Life, The Immune System Company
®, and the first to bring transfer factor research to market, has offices in dozens of countries to serve the company’s worldwide customers.
For more information:
Calvin Jolley
Vice President Corporate Communications
4Life Research
[email protected]
