1. Start with Exceptional Formulas.

Each Altrient® formula spends at least 24 months in research and development, with formulators who have over 25 years of experience in Liposomal Encapsulation Technology (LET). This may be longer than most liposomal products spend in R&D, but LivOn know this is how long it takes to formulate, make samples and properly monitor the stability of a good formula.

Before a formula is approved, multiple samples of the formula are made using our patented cold process for manufacturing liposomal supplements. Samples are tested at regular intervals for active ingredient content, changes in consistency, and encapsulation efficiency of the active nutrient. After a formula passes the initial testing, larger test batches are made and packaged for long term stability monitoring.

When a formula is finally approved, LivOn are confident it will consistently produce a highly stable liposomal product, with significant encapsulation efficiency and is guaranteed to meet the label claims to the end of its expiry date.

2. Use High Quality Ingredients.

Every Altrient® product is made with ingredients that are 100% non-GMO, hexane-free, gluten-free, sugar-free, and free of pesticides.

LivOn only work with well-known, qualified suppliers who can provide written proof that each ingredient is made from non-GMO materials. To verify the materials are non-GMO, LivOn routinely test each product for DNA markers. LivOn also require proof that strict quality processes are followed to maintain the integrity of the ingredient.

LivOn use the best ingredients available so you can feel safe taking Altrient® supplements every day.

3. Test Everything.

LivOn are dedicated to some of the most demanding safety and quality standards in the industry. LivOn manufacture Altrient in the USA, in facilities that are routinely inspected by the FDA and certified by NSF International for compliance with current Good Manufacturing Practices (cGMP). Throughout production and packaging, each batch is monitored and tested at critical points for active ingredient content, microbiological agents, heavy metals, and other potential contaminants. Each test is performed in qualified laboratories, using analytical methods that have been approved by nationally recognized organizations like the Association of Analytical Communities (AOAC) and United States Pharmacopeia (USP).

After each batch is packaged, LivOn evaluate the physical characteristics of each sample, and conduct an additional round of microbiological testing. Finished products are only released after the quality control team team has thoroughly reviewed all of the batch records and determined the product meets our specifications.