Quality & Compliance
NSF/ANSI 455-2 GMP for Dietary Supplements listed facilities.
Our facilities are NSF/ANSI 455-2 GMP for Dietary Supplements listed, third-party testing is part of every program, and a quality unit oversees each run from components to release.
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NSF/ANSI 455-2 GMP for Dietary Supplements
Our facilities are NSF/ANSI 455-2 GMP for Dietary Supplements listed — the GMP standard many retailers ask their suppliers for.
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Quality unit operations
A quality unit oversees specifications, component and material review, in-process checks, packaging and labeling controls, deviation handling, and release of finished goods against the approved specification.
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Third-party testing
Third-party testing is part of every program. Certificates of analysis and specification documents are shared with you during approval.
What NSF/ANSI 455-2 means for your brand
NSF/ANSI 455-2 is the good manufacturing practice (GMP) audit standard for dietary supplements. It was developed with retailers and industry to give them one consistent GMP audit, built on the FDA's dietary supplement GMP rule (21 CFR Part 111).
For you, it means the facilities that package your product are independently audited against the standard many retailers ask their suppliers for, and that the documentation a buyer expects already exists.
What third-party testing covers
Third-party testing checks the finished product against its approved specification. Depending on the product, that commonly includes identity, the amounts of key ingredients against label claims, microbiological limits and contaminants such as heavy metals.
The exact tests, methods and acceptance criteria are agreed for each program, so you know before the run what will be tested and what passes.
Documents you receive
- Certificates of analysis for your product
- Finished product and packaging specification documents
- Approved artwork and prototype sign-off for the finished pack
These are shared with you during approval, and reorders run against the same approved specification.
Product formats
Formats we work with
Explore each format to see packaging options, configurations and what to send us for a quote.
Questions
Quality & compliance FAQ
Bottles and jars, stand-up and flat pouches, stick packs, liquid bottles, cartons and retail displays — for gummies, capsules, softgels, tablets, powders, soft chews, lozenges, lollipops and liquids.
Yes. You can buy bulk product from our sister company, RV Pharma, and we'll package it or private label it under your brand. See vitaglobe.com for an example of a finished program.
Browse RV Pharma's bulk catalog →Yes. We hold a working stock of bottles, closures and cartons, with label die lines on file for every packer bottle we stock. Anything outside our stock can be sourced to your spec.
Yes. We make a physical prototype — bottle, closure, label and carton — so you can review it in hand before you approve the run.
Yes. We work through the label layout with you — brand panel, Supplement Facts, directions and other approved copy — before anything goes to print. Final regulatory wording should be confirmed with your regulatory advisor.
Yes. Case packs, inner packs, labeling, shelf-ready displays and pallet configurations are built to your retailer's packing instructions.
Yes. Third-party testing is part of every program, and certificates of analysis are shared with you during approval.
Yes. 1/4 gram silica gel desiccants, scoops and leaflets can be added during packout.
Yes. We can include formulation in your program, so the product and the packaging are planned together.
Yes. Finished goods are warehoused and shipped from our fulfillment plant to your 3PL, retail distribution centers or straight to your accounts.
Your format, count or fill weight per pack, preferred packaging, estimated quantity, timeline and any retailer requirements.
Have a question that's not here?
Request a Quote →Tell us the product you want on the shelf.
Send format, estimated quantity and timeline. We will come back with the packaging path and what it takes to run it.