Education & Training

Fullscript onboarding tools

Step-by-step guidance for onboarding your team and integrating Fullscript into your clinical workflow.

Getting started with Fullscript

Training videos designed to help providers and staff use Fullscript confidently at the point of care.

Fullscript Quality Standards

A four-tier quality system behind every product on the platform. Continuous verification, independent finished-product testing, and clinical behavior data. Every SKU must clear this baseline, and keep clearing it. Third-party cGMP certification verified for every brand and contract manufacturer (CDMO), with ongoing documentation review. Products stored in NSF cGMP-certified, FDA-registered facilities.

Continuous cGMP monitoring
CDMO documentation review
Verified COAs
NSF-certified, FDA-registered storage

Fullscript Enhanced Tested

Fullscript-funded independent finished-product testing. ~100 SKUs per quarter, selected by our clinical team. Brands have no influence. Products must demonstrate 100% of label claims for potency and meet Fullscript's purity thresholds. Failures trigger root cause investigation, quarantine, and catalog removal until independently retested.

~100 SKUs/quarter
Independent labs · staff blinded
Brands don't nominate
Valid 1 year, then retest
Outcomes published annually

Selection

Prioritized by formulation risk, adulteration history, and intelligence from industry and academic sources on emerging concerns.

Potency threshold

100% of label claims confirmed by independent third-party lab.

Sampling

Samples pulled from Fullscript distribution centers. Brands cannot nominate or submit their own.

Purity

Heavy metals, microbial, and novel contaminants. Fullscript holds brands to stricter microbial thresholds than industry standards.