Utah 7-Hydroxymitragynine Compliance: Part Number 801
1/30/2026
Part Number 801 (7-Hydroxymitragynine Relative Alkaloid Ratio) supports Utah SB0048 ratio-based compliance reporting for 7-OH.
Resources
Clear, practical guidance on testing options, common specifications, and how to build a panel that matches your product and market needs.
Explore
Choose a resource
Each section is focused, so you can jump straight to what you need.
Viewing: News + Updates
News and updates
Announcements, regulatory updates, and lab news.
Austin Weather Update: Potential Service Delays
1/23/2026
Inclement weather and power outages in Austin may impact turnaround times through Monday. Contact your account manager or one of our help inboxes with questions.
Florida 7‑Hydroxymitragynine Update
10/7/2025
Florida sets a 400 ppm (0.04%) dry‑weight limit for 7‑OH and requires ppm labeling. Cora Science Test Code 813 adds moisture analysis and reports dry‑weight‑corrected 7‑OH in ppm.
Customer FAQ
Common questions about panels, specifications, and turnaround.
How do I choose between standard and expanded panels?
Standard panels cover the core compliance needs for most products. Expanded panels add category-specific testing like residual solvents, mycotoxins, or additional analytes. If you are unsure, we can recommend a starting panel based on your product and target market.
Which official specifications do you follow?
We commonly reference USP chapters (for example <467>,<561>, <61>,<62>), AOAC methods, and FDA BAM guidance when applicable. The final specification depends on product type and regulatory requirements.
What sample information should I provide?
Provide the product type, lot ID, matrix, target analytes, and any known processing details (such as solvent extraction or preservatives). This helps us confirm the most appropriate methods.
What is typical turnaround time?
Turnaround varies by panel and sample type. Most routine panels are completed within a standard lab schedule, and rush options may be available upon request.
Do you support ISO/IEC 17025 testing?
Yes. Our quality system aligns with ISO/IEC 17025:2017, and we can provide additional documentation as needed.
How do I request a quote or custom panel?
Start with the contact form, and we will follow up with a tailored scope and timeline.
Specification Selector
Explore common official references based on product type and testing needs.
Step 1
Choose a product type
This sets a baseline panel aligned to the product format.
Step 2
Add considerations
These options layer additional official references onto the baseline.
Step 3
Official references
A consolidated list of references based on your selections.
- USP–NF (purchase/access)USP · public
- AHPA Guidance Policies (index)AHPA · public
- AOAC Official Methods of Analysis (OMA)AOAC · public
- USP <561> Articles of Botanical OriginUSP · paywalled-preview
- AHPA: Heavy Metals policyAHPA · public
- AOAC OMA: Search by MethodAOAC · public
- FDA Mycotoxins (overview & action levels)FDA · public
- AHPA: Recommended Microbial Limits for Botanical IngredientsAHPA · public
Optional add-ons
Add any modules that apply to your product, even if they are not in the baseline.
Compliance checklist
Track coverage of the core requirements tied to your selected panel.
Identity and potency
Confirm product identity and label claims are supported.
Contaminants and residues
Address safety risks tied to botanical inputs and processing.
Microbiology and preservation
Verify microbial safety and preservative effectiveness.
Regulatory alerts by category
Topics commonly monitored for your product category. Confirm with your compliance team for jurisdiction-specific requirements.
Botanical guidance updates
Monitor AHPA and USP botanical guidance updates that can influence testing scope.
This tool is a guide for common specifications and does not replace regulatory or legal review. Requirements can vary by ingredient, product claims, and market.
Research digest
Subscribe for periodic updates on botanical testing and lab research.