Standards

Before you Order our Products for Fibromyalgia  from the fibromyalgia Treatment Center we want you to know more about our fibromyalgia medication standards. There are 1037 manufacturing facilities in the USA.  The lab and manufacturing plant  we chose uses a rigorous 7 step examination to produce the highest Medication Standards for FIBROMYALGIA products.  We want to provide you with the safest and most effective alternative fibromyalgia medication products. 


Less than ½ of 1% of the nutritional manufacturing facilities in the US match the precise standards followed by our facility.  Our products are manufactured in a lab that follows standards beyond those suggested under Good Manufacturing Procedure (GMP) guidelines, giving our products a Fibromyalgia Medication Guarantee.

Precise Environmental fibromyalgia Medication Standards
Each room has its own air handler that completely exchanges the air 50 times per hour.  Pure, clean air is a critical element in manufacturing a pure product.  There are so many contaminants in the air that a state of the art air scrubbing system is a necessity.  Many facilities have just a dust handler, relying on the air conditioning system to fight to replace the air.  You might as well make the product in the parking lot.  The temperature is at a constant 71 degrees and the humidity is less than 35%.

Particle Sizing For Better Absorbency
The key element of our manufacturing process is particle sizing.  Simply put, all of the elements come in different particle sizes.  Imagine tennis balls, ping-pong balls, golf balls, baseballs, softballs, and basketballs. Improper mixing yields batches that have all of the basketballs at the top and the tennis balls at the bottom. This would mean that each capsule has a different mix of ingredients (those early in the loading process would have too many basketballs).  We use cold process pulverization to take all particles to the same size so everything is similar.  Smaller particle size means that the body assimilates the elements more readily.

Capsules have Longer Lasting Potency
The product is weighed and blended in a static, gravity free environment.  This incorporates 100% batch involvement in the mixing process with no dead spots. While in the blending process, the ambient air has been removed and replaced with stable nitrogen, which is heavier than air and reduces oxidation and process contamination.  The bulk material is weight validated to assure batch size compliance, then formulation and quality control verified for batch uniformity. The lab signs off on weight sheets to make sure that everything that was supposed to go in, went in.

Vigorous Qualitative Analysis
In the Encapsulation Department, pharmaceutical standard, GMP certified machines employ the dose tamping method.  Powder goes into the machine then is tamped with pins into the capsule to the milligram of accuracy. This process is done one capsule at a time.  During this process, at 5 minute intervals, a person will test to validate quantities.  The capsules are polished, dust is removed, and they are hand inspected to see that they are not dented, scratched, or broken. The finished product is analyzed using high-pressure liquid chromatography, which creates a quantitative analysis of a compound.  Then a mass spectrometer is used to create a qualitative analysis.  This creates the blue print that all future capsules must match.

Every Capsule Within a 1% Weight Tolerance
At the end of the production process, checks are run to insure that the product weighs what it should. Industry standards allow +/- 5% failure tolerances. We insist on a tolerance of +/- 1%. Many manufacturers cut corners here.  It is in their interest to do so as 5% less material in each capsule adds up to serious costs saved over time.

Highest Quality Control Standards
In the end, each batch comes with a certificate of analysis and has a National Drug Control number.  Once it is manufactured and packaged, the product is then tested by lot to ensure quality control, stability, consistency, weight, and content.  Time series and dating analysis are performed twice on all lots, first at the lab and then when received as a finished product.  Strict controls of inventory dating and ongoing computer evaluations are performed daily, while total rechecks of inventory are performed each month.

Do not compromise on the products to improve your health.  We suggest you use products with  the highest  Fibromyalgia Medication Standards.