Nutraceutical & Supplement Labs
Dietary supplement and botanical labs verify identity, potency, and contaminants against label claims and cGMP expectations. Aliquora gives you structured testing and traceable release — without an enterprise rollout.
What Aliquora handles for Nutraceuticals
- Track raw botanicals, blends, and finished supplements by lot
- Flag potency and contaminant results against label claims and limits
- Review and approval workflow before lot release
- Generate COAs with your lab's branding
- Audit log support for data integrity
How it works
A typical nutraceuticals workflow in Aliquora
- 1
Log the lot with its label context
Register each raw material, in-process blend, or finished supplement with its lot number, dosage form, and the label claim it will be tested against. Linking the sample to its claim keeps verification traceable.
- 2
Assign identity, potency, and contaminant tests
Select the panel — botanical identity, active potency, heavy metals, microbials, or contaminants. Specification ranges and label-claim targets are configured per test so every result is evaluated consistently.
- 3
Enter or import results
Enter assay readings manually or upload an instrument CSV. Aliquora compares each value to its configured limit or label claim and flags any shortfall or exceedance on entry.
- 4
Investigate and disposition
A potency shortfall or a heavy-metal exceedance holds the lot until an analyst records the investigation outcome — retest, confirmed result, or justified override. The audit log captures every step.
- 5
Approve and issue the COA
An authorized reviewer signs off with password re-confirmation. Aliquora generates a branded PDF Certificate of Analysis listing each test, its specification, and pass/fail status for the lot.
Supplement labs working under 21 CFR Part 111 cGMPs need documented identity and specification testing with traceable release records. Aliquora's audit log records every entry, edit, and approval with a timestamp and user identity. Note: full 21 CFR Part 11 compliance requires a validated system — consult your quality team before use in a regulated context.
Frequently asked questions
- Can we test finished products against label claims?
- Yes. Each test type carries a configured target or limit — including label-claim potency — so Aliquora automatically flags any result that falls short of or exceeds what the label states.
- Does Aliquora support identity and contaminant testing?
- You define your own test types, so botanical identity, active potency, heavy metals, and microbial limits are all configurable with their own specs, units, and pass/fail criteria.
- Does this help with 21 CFR Part 111 recordkeeping?
- Aliquora provides traceable records of who tested, reviewed, and approved each lot, with an audit log of all data entries and edits. Full regulatory compliance still requires your own validated processes — consult your quality team.
- Can we brand the COA for our customers?
- Yes. COA PDFs include your lab name and contact information, and custom logo support is available on paid plans.
Other lab types
See how Aliquora works for Nutraceuticals
Start your free trial and we'll help you get set up. No long contracts, no six-month deployment.