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 Our manufacturer is exceptionally demanding of superior quality throughout every step of the manufacturing process. Each and every raw material which enters the building is inspected for approval. Written Standard Operating Procedures (SOP's) for each aspect of production are meticulously followed to adhere to strict in-process quality control standards during product manufacturing. In the initial stages of production, stringent testing and sampling must be conducted before any further production cycles may continue. Accuracy is an absolute must. Records are kept of each component and the quantity used in every batch of product.
Our manufacturer takes great pride in our uncompromising approach to providing you with the product which meets, and often exceeds, USP standards. The facility is routinely inspected by the FDA as well as representative companies from Canada and Europe and we are also proud to be approved as a nutritional supplement manufacturer by the Canadian Health Organization and the Commission of the European Communities. Before the Arterial Cleansing Formula is offered for sale, it must pass as many as 37 individual laboratory tests, consisting of:
Arterial Cleansing Formula is certified by an independent laboratory to meet the stringent testing oulined. This ensures that consumers receive the highest quality, contaminant-free product.
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| © 1998-2003 Atherosclerosis Controlled Nutritionally At 50+. Arterial Cleansing Formula - Reverse Atherosclerosis Withut Drugs or Surgery. All rights reserved worldwide. This document may not be copied in part or full without express written permission from the publisher. The information on atherosclerosis and nutrition provided herein is a general overview on this topic and may not apply to everyone, therefore, it should not be used for diagnosis or treatment of any medical condition. While reasonable effort has been made to ensure the accuracy of the information on atherosclerosis, Full-Health.com assumes no responsibility for errors or omissions, or for damages resulting from use of the information herein. | ||||||
Testing laboratories, under the supervision of our in-house Ph.D, precisely monitor the production cycle. Chemical Analysis Lab carefully checks bioavailability with USP dissolution tests and pH testing while verifying potency with high pressure liquid chromotography (HPLC). This ensures that your supplement will not contain less than 100% of the label claim. The Physical Analysis Lab checks the weight, hardness and thickness for consistency on the tablets. It is this process that guarantees constant integrity of each formulation. To meet the USP microbiological limit requirements for nutritional supplements in the USP XXIII, the Microbiology Lab conducts microbial testing on all products. The final products are then kept in tightly controlled conditions of light, temperature and humidity for optimal freshness.
