Label Claim and Quality processes

Label Claim and Quality processes

Our entire manufacturing process follows a rigorous documented process overseen by your Quality Assurance Team and Quality Control Team. Every step of the process is documented and signed per FDA 21 CFR Part 111. We are audited by UL and NSF and brand owners.

A big part of our encapsulation services is to get a perfect blend into each capsule. We have multiple blenders available on location from 50kg to 300kg to 1000kg. We analyze each formula to determine the right overages in order to get the right amount of each active into every single capsule.

Each raw material is different, and it requires a different overage. We have our own internal laboratory where we test your raw materials at multiple points. We test your finished goods for potency, identity, and purity. Having our own lab results in shorter lead times. Our 3rd party potency testing is done with Eurofins and Dyad Labs.

PureNSM quality control
GMP Flow Chart
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