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Contact:

Relentless Improvement LLC

PO Box 19220
Reno NV 89511 USA
info@RelentlessImprovement.com

Phone orders require $100 minimum order, no exceptions. We no longer accept mail orders.

(925) 294-5795 (M/F 8:30AM-12PM Pacific)
(925) 905-2919 FAX

Phone orders require $100 minimum order, no exceptions. We no longer accept mail orders.

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No statements on this site have been evaluated by the FDA. These products are not intended to diagnose, treat, cure, or prevent any disease.

Certficates of Analysis

Relentless Improvement brand products are offered with third party Certificates of Analysis derived from expensive, time-consuming, finished product testing. Only a small handful of companies worldwide provide this degree of product quality assurance and public disclosure.

No laws or regulations require us to document the quality of our products, we choose to do business this way so that you may have the ultimate level of confidence in our supplements.

FDA registered, USA based analytical testing laboratories are used for all of our product testing. Manufacturer's Certificates of Analysis, unfortunately, are not always reliable and frequently lack key quality assurance controls and information.

Relentless Improvement is not required to adhere to CA Proposition 65, but we test as if we were for the peace of mind of our customers. (Proposition 65 was passed over 10 years ago by the voters in California and established California-only allowable levels of daily ingestion of four heavy metals)

Relentless Improvement brand supplements exceed in every measure the most conservative guidelines of Califormia Proposition 65 requirement. These are the most stringent of any state.

Our public CoA's tie back to the exact product we are shipping to you, and usually note the finished product lot number. They are properly dated, signed, and publicly identified with our address information and testing laboratory information for that specific product.

Relentless Improvement brand documented products are your key to safety and efficacy and meet/exceed all FDA, WHO and California Prop 65 standards for claimed label content, sterility and freedom from heavy metal contaminants.

Consider and understand this additional fact: A molecule does not know in which country it was manufactured. Any country is capable of manufacturing high and low quality materials. Furthermore, a high quality raw material might acquire a contaminant in the encapsulation/bottling process.

So don't ask where the raw material was manufactured. It doesn't matter. What does matter is the quality of the bottled finished product.

Click on the product name below to view the CoA in PDF format for what is currently shipping to you.

Alpha-GPC (Choline Alfoscerate) Pharmaceutical purity. Exceeds all standards.

Carnosine Eye Drops Pharmaceutical grade, full potency, documented sterile.

Centrophenoxine (Meclofenoxate) Pharmaceutical purity, exceeds all standards, metals well under limits.

EgCG Green Tea SuperPotent Extract True pharmaceutical grade, ultra-pure, free of residual solvents.

Galantamine Pharmaceutical purity, exceeds all standards, metals well under limits.

Idebenone Per capsule mg exceeds label claim. More value for you.

Iodine/Iodide High Potency Complex Relentless Improvement Iodine/Iodide supplement exceeds in every measure the most conservative guidelines of Califormia Proposition 65 requirement. These are the most stringent of any state.

K2 menatetrenone Tests to full potency and exceeds all standards of purity.

Oxiracetam Pharmaceutical purity exceeds all standards.

Phenibut Pharmaceutical purity.

Picamilon Purity exceeds all standards. Picamilon reference standard not available, therefore not tested for mg active material.

Piracetam Ultra-purity. No detectable microbial/molds/yeasts. Metals levels documented to the lowest amount that can be practicably obtained in manufacturing (for example lead, which is 93% less than the 10ppm USP proposed allowable).

Sulbutiamine A documented pharmaceutical grade.