Quality Control

Since 1995, BodyBio® has used only the purest raw materials available, and has implemented strict quality control procedures in every stage of production, including inspection of raw materials, manufacturing, packaging, and storing. BodyBio is NSF Certified, the foremost Public Health and Safety Organization in the United States. We follow the cGMPs set forth by the NSF and adhere to the strictest regulations ranging from extensive product testing and material analyses to plant inspections. Every aspect of BodyBio has been thoroughly evaluated in order for us to earn NSF certification. BodyBio is licensed under the US FDA registration number 10025648778.

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GMP Standards

Our products are manufactured under GMP requirements in NSF/ANSI Standard 173, section 8 and comply with Dietary Supplement current Good Manufacturing Practices (cGMP). The GMP standards are applied to a wide variety of procedures associated with the manufacturing of dietary supplements, including receiving, testing, and approval of raw materials, production, and process controls, laboratory testing of labeled and packaged finished product, distribution control and accountability, and shelf life expiration testing to ensure freshness and potency.  For the products that we do not physically manufacture in-house, we have spent years getting directly to the source of the purest and highest quality available. We ensure that our certified manufacturers meet or exceed cGMP requirements established by the FDA, as well as state and local regulations. All of the products and packaging are tested at our in-house QC facility as well as send it out for third party testing and verification.  In our facility in Millville, New Jersey, our highly trained staff produce, bottle, label, and ship our finished products.


Independent Third Party Laboratories

In addition to our in-house quality control department, we use certified independent analytical laboratories to test raw materials as well as finished products. All of our certified laboratories meet or exceed cGMP requirements. Our products are assayed for identity, purity and potency, and are confirmed to contain predetermined amounts of the contents listed on every label. Microbial, pesticides/herbicides, aflatoxins, residual solvents, and heavy metals analysis are also conducted on all applicable products.


Procedures of Analysis

We utilize a number of advanced methods of analysis, including Fourier transform infrared spectroscopy (FTIR) at our in-house QC. We send out for high performance liquid chromatography (HPLC), inductively coupled plasma-mass spectrometry (ICP-MS), gas chromatography (GC), DNA analysis, GMO-Testing, major food allergen testing, and radiation contamination testing along with biochemistry and wet chemistry techniques.