GMP Manufacturing

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GMP, or Good Manufacturing Practices, is a term that is recognized worldwide for the control and management of manufacturing and quality control testing of foods and pharmaceutical products.

 

So what is it?  Like ISO9000 standards, GMP is a comprehensive list of requirements for manufacturing and testing processes and their correct documentation.

 

The US FDA (Food and Drug Administration) publishes and enforces these guidelines in the United States.

 

More details.  GMP takes the holistic approach of regulating manufacturing and laboratory testing environments. An extremely important part of GMP is documentation of every aspect of the process, activities, and operations involved with drug and medical device manufacture. If the documentation showing how the product was made and tested is not correct and in order, then the product does not meet the required specification and is considered adulterated.  Additionally, GMP requires that all manufacturing and testing equipment has been qualified as suitable for use, and that all operational methodologies and procedures utilized in the manufacturing process have been validated, to demonstrate that they can perform their purported function(s).

 

MendRight Joint Patches are manufactured with GMP processes.

Source of Ingredients

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Raw materials for MendRight Joint Patches are procured from the largest and most reputable material suppliers in the United States.  These suppliers are also subject to US FDA GMP requirements. Joint Patch ingredients are only sourced from GMP suppliers. 

 

Made in USA

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MendRight Products are made in the USA.