The NeoLife Difference

Nov 20

Created by Doctors and Scientists

The NeoLife Scientific Advisory Board (SAB) sits at the helm of NeoLife’s product strategy and development, ensuring each and every one of our leading-edge formulas are based in nature and backed by science, using only the finest and safest ingredients. The SAB is made up of world class doctors, scientists and health experts who share our commitment to end the trend.

Meet Our SAB

Whole Food Based Cellular Nutrition

For over 60 years, generations of families around the world have counted on NeoLife to do what no other company can do: produce products that are based on the finest whole food, human food chain ingredients and proven effective by millions of satisfied customers.

Since we are only as healthy as our cells, we use only the most bio-efficient forms of nutrients to maximize nutrient absorption, utilization and benefit to the body.

Non-GMO

NeoLife products use only GMO-free ingredients and are routinely tested for potential contaminants. NeoLife requires that suppliers and manufacturers guarantee that all raw materials are free from genetically modified DNA and genetically modified organisms. We then validate and closely monitor each and every ingredient in our laboratories and manufacturing facilities.

Full Traceability from Farm to table

https://focus.neolife.com/blog/full-traceability-farm-to-table/

Our state-of-the-art quality assurance program includes these 10 steps for full traceability from farm to table.

1. Meticulous Seed Selection
2. Pristine Soil & Environment
3. Field Crop Monitoring
4. Nutrient Optimizing Harvest
5. Quality Control Raw Crop Analysis
6. Nutrient Extraction & Concentration
7. Purity & Potency Verification
8. Socially Responsible Manufacturing
9. Quality Control & Laboratory Analysis
10. Product Delivery & Batch Tracking

Read more about how NeoLife’s Full Traceability process works.

https://focus.neolife.com/blog/full-traceability-farm-to-table/

Clinically proven human clinical studies

Human clinical studies proving the effectiveness of NeoLife products have been published in some of the world’s most prestigious scientific journals including the Journal of the American College of Nutrition, the International Journal of Toxicology, the FASEB Journal, and the American Journal of Clinical Nutrition.

Human clinical studies are a unique point of pride for NeoLife, in a world where yeast and animal studies remain the predominant choice. NeoLife continues to research and publish studies for breakthrough supplements and organic skin care.

Look for the when shopping products to see abstracts of related studies.

Pharmaceutical License for Manufacturing and Why It Matters:

NeoLife owns and operates state-of-the-art manufacturing facilities that surpass the most stringent global GMP standards and manufacturing regulations.

This includes a Drug License from the State of California as well as the esteemed Drug License from the TGA of Australia, which very few manufacturers in the United States are able to obtain. Although we do not manufacture drugs, we hold these licenses and others as validation of our exceptional quality standards.

We are registered with the FDA and operate under their regulation and compliance.

When a vitamin or supplement manufacturer holds a pharmaceutical license, it means they’re approved to operate under the same strict regulatory standards that govern drug production. Here’s why that matters:

Higher manufacturing standards:
Pharmaceutical licensing requires compliance with Good Manufacturing Practices (GMP) for medicines, not just supplements. That means tighter control over cleanliness, equipment calibration, raw material quality, and documentation.
Quality and consistency:
Every batch must meet precise standards for purity, potency, and composition — so what’s on the label is exactly what’s in the bottle. This level of consistency is often far above what’s legally required for standard supplements.
Testing and validation:
Licensed pharmaceutical facilities are typically required to conduct rigorous testing for contaminants, stability, and efficacy, sometimes including third-party verification.
Regulatory oversight:
The company is inspected and audited by health authorities (for example, the FDA in the U.S. or MHRA in the U.K.), ensuring ongoing compliance and transparency.
Reputation and trust:
A pharmaceutical license signals to consumers, healthcare professionals, and partners that the company’s products are made under conditions comparable to prescription medicines — which can build significant credibility.

In short, it means the company’s vitamins are being produced under a drug-level standard of quality and safety, which is unusual in the supplement industry.

Strategic Partnerships

NeoLife's reputation for scientific excellence is so well established that our products have been used by researchers from such renowned bodies such as the United States Department of Agriculture, UNESCO, and major universities and scientific institutions around the world. NeoLife has been able to partner with the Stanford University Health Library to produce the annual NeoLife-Arthur Furst Lecture Series on Nutrition & Disease Prevention. NeoLife is a founding member and remains a major contributor to the Polyphenols in Human Health Research Interest Group (PhenHRIG). In 2019, NeoLife was also a proud contributor to the 10th Linus Pauling Institute International Conference. For over 25 years, we have partnered with the University of San Francisco to award the annual Arthur Furst Undergraduate Scholarship.

NeoLife is also a Member of the Council for Responsible Nutrition.

Through these ongoing programs, NeoLife is changing the face of health care and disease prevention through nutrition by actively supporting today’s scientists and tomorrow’s doctors.