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Licensed Research: Solo-Chemist Supplement Build
Publicly online since 2010 · U.S. patent applications since 2012 · inventions offered since 2014. The work of Christopher Gabriel Brown, independently documented.
| Product | Licensed Research: The Solo-Chemist Supplement Build |
| Format | Downloadable toolkit — guide + two outreach templates + an ingredient checklist, delivered as a ZIP right after checkout |
| Subject | Turning a formula into a lawful dietary supplement with a single chemist |
| Worked example | A diabetes “metabolic support” blend — structure/function support, not a cure |
| IP posture | Patent Pending — metal–amino-acid formulations & methods |
| Author | Christopher Gabriel Brown, Lawrenceville, GA, USA |
| License fee | $1,495.00 USD — Licensed transfer |
01 What is inside the toolkit
- The Solo-Chemist Supplement Build — the full illustrated guide.
- Outreach template #1 — ready to send to a formulation chemist / compounding pharmacist.
- Outreach template #2 — ready to send to a 21 CFR Part 111 contract manufacturer.
- Ingredient sourcing checklist — the forms to order, target doses, and the safety caps.
Delivered as a single downloadable ZIP the moment your order is placed.
02 The team — your “one chemist”
The whole trick is that you do not synthesize anything — every ingredient already exists as a USP/food-grade raw material you simply buy. So the real job is formulate → source → have it made → label honestly, and that genuinely is a one-chemist operation:
- You — the formula concept and IP holder.
- One formulation chemist or compounding pharmacist (contract/consulting) — finalizes the formula, forms, and doses, and writes the spec. This is the single chemist.
- A 21 CFR Part 111 contract manufacturer — does the actual blending, encapsulation, and QC. They already have the bench chemists and lines, so you build nothing.
03 The six steps, formula to shelf
| 1 | The formulation chemist finalizes the formula, doses, and capsule form within safe upper limits. |
| 2 | Source COA’d (certificate-of-analysis) USP/food-grade raw materials from established suppliers. |
| 3 | File an NDI notification only if an ingredient is post-Oct-1994 / novel — standard chelates are not. |
| 4 | The Part 111 contract manufacturer blends, encapsulates, tests (identity, purity, heavy metals), and returns a batch record + COA. |
| 5 | Label per 21 CFR 101: Supplement Facts panel, structure/function claims only + the FDA disclaimer; notify the FDA within 30 days of first using a claim. |
| 6 | You hold safety responsibility and serious-adverse-event reporting. |
04 What you may — and may not — say
| Allowed (structure/function) | Not allowed (disease claims) |
| “Supports healthy glucose metabolism.” “Supports healthy insulin sensitivity.” “A source of zinc & magnesium for normal carbohydrate metabolism.” | “Treats / cures / reverses diabetes.” “Lowers blood sugar.” “For diabetics.” |
Required on every claim: “This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.”
1341 Wellington Cove, Lawrenceville, GA 30043-5255, USA
Email and postal mail only — no phone calls, please.
Educational, plain-language toolkit about the lawful dietary-supplement pathway. Not legal, medical, or regulatory advice; not affiliated with or endorsed by the FDA. Dietary supplements are regulated under DSHEA: structure/function claims require the FDA disclaimer above and may not claim to diagnose, treat, cure, or prevent any disease. Confirm NAC’s current FDA enforcement-discretion status, and all 21 CFR Part 111/101 requirements, with a qualified formulation chemist and a supplement attorney before manufacturing or labeling anything. Rules, forms, and fees change — always verify against current FDA guidance.
© 2026 Christopher Gabriel Brown. All rights reserved. “Cri-One” and “Licensed Research” are product designations of the licensor. Patents retained; not sold.
