Isoquercetin: a form the body prefers. The Leading Edge: a review of our new high-tech distribution center Protocol: Aging and Healthy Metabolism Tell us what you think: Your feedback matters. Login

A Legacy of Quality

ITI is one of only a select few dietary supplement manufacturers that are in full compliance with GMPs that have already been established for drug manufacturing facilities. Currently these standards are much more complex and rigorous than those expected for dietary supplement manufacturers.

ITI conducts more than 35,000 tests on its products every year. The laboratory staff is extremely knowledgeable regarding analytical methodology for botanicals and other nutrients. They have published research papers in respected peer-reviewed journals.

ITI monitors and tests ingredients at various points during the manufacturing process. Before any raw material is processed, it must pass through a "quarantine" period. As part of this inspection process, ITI scientists use a variety of test methods, including High Performance Liquid Chromatography (HPLC), Atomic Absorption Spectroscopy (AA), and other chromatographic techniques, along with microbiological analysis, to ensure the purity of every ingredient. Lab analysis confirms ITI is using the correct plant and getting the right quality and quantity of chemical constituents. These analyses makes certain that bacteria have not contaminated the raw materials. Raw materials are also examined for contamination with pesticides or other toxins.

Type

Test

What it does

Accuracy

High Performance Liquid Chromatography (HPLC)

Tests for presence and quantity of active ingredients

Accuracy

Atomic Absorption

Tests for presence and quantity of minerals

Accuracy

Gas Chromatography

Verifies the chemical nature of compounds

Accuracy

Fourier Transform Infrared (FTIR)

Tests for unique "chemical fingerprints" to identify products

Safety

Vendor Qualification Program

In-house laboratory testing ensures vendors always provide safe ingredients

Safety

Internal Audit Program

Quality Assurance conducts manufacturing audits to ensure all products are made safely

Safety

Microbiological testing

Identifies bacterial, mold, and fungal contamination

Usability

Organoleptic tests

Sensory tests for appearance, odor, and taste

Usability

Hardness testing

Ensures chewable tablets are comfortably chewed as they age

Usability

Friability

Verifies the tablet stays intact in the bottle without breaking during handling or shipping

Usability

Disintegration, Dissolution

Ensures that the tablet or capsule dissolves in the body so that active ingredients are bioavailable; performed according to standards specified by the United States Pharmacopoeia

Process validation studies ensure that the written process approved for each product performs consistently from batch to batch. Cleaning validation studies ensure that no residues from products, harmful microbes, or cleaning/sanitizing products remain on the equipment. ITI's cleaning validation program was modeled after the standards maintained in drug manufacturing facilities.

ITI products include ingredients derived from a variety of extraction processes, including hot water extraction, alcohol extraction and super critical CO2 extraction, to name a few. We at no time accept any raw material extracted with solvents that have shown adverse health effects.

Get the Flash Player to see this player.
We began as seeds planted over 30 years ago…

NF Formulas, PhytoPharmica®, Tyler Encapsulations and Vitaline® Formulas.

Over the years, we have matured to form one company, Integrative Therapeutics, well-known for developing the most effective, proven natural health solutions in the industry. We take great pride in our unique combination of science and nature, and trust that you’ll turn to us time and again for cutting-edge, health-enhancing supplements.

Most importantly, at the forefront of everything we do, is our unwavering commitment to quality. When Results Matter™, you can feel confident that you’ve made the right choice with ITI.