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ISO 17025 Accredited

Nutraceutical Testing for Product launch

Reliable nutraceutical testing designed for product launch. ISO 17025 accredited methods with detailed reporting to meet your regulatory requirements.

ISO 17025 Accredited 48-Hour Turnaround Available 500+ Test Methods FDA-Compliant Reporting Dual Locations: Irvine & San Diego, CA

Quick Answer

Nutraceutical Testing for product launch ensures products meet the specific regulatory and quality standards required for market entry. ISO 17025 accredited laboratories like Qalitex provide validated testing methods, detailed COA reports, and expert guidance to support product launch processes efficiently.

Achieving product launch requires accurate, accredited laboratory testing that regulatory bodies and marketplace platforms trust. Qalitex Laboratories provides nutraceutical testing tailored for product launch requirements. Nutraceuticals occupy the space between food and medicine — requiring testing rigor that meets both FDA dietary supplement regulations and food safety standards. Qalitex Laboratories provides full-spectrum nutraceutical testing programs tailored to your specific formulation, target market, and regulatory needs. Our ISO 17025 accredited methods and detailed COA reports are designed to streamline your product launch process.

How Nutraceutical Testing Supports Product launch

Product launch requires documented evidence of product safety and quality. Qalitex provides the specific testing and documentation needed to support your product launch process, including detailed COA reports, method validation documentation, and expert consultation on testing scope. Our ISO 17025 accreditation ensures your results are accepted by regulatory bodies and marketplace platforms.

Full-Spectrum Testing Program

Our nutraceutical testing covers the full quality lifecycle: raw material testing, in-process testing, finished product release testing, and ongoing stability studies. We coordinate testing programs for brands launching new formulations or maintaining compliance for established products.

Bioactive Ingredient Testing

We quantify bioactive compounds including polyphenols, flavonoids, antioxidants, omega fatty acids, carotenoids, and other functional ingredients using validated HPLC, GC, and spectroscopic methods.

Regulatory Compliance Support

We provide testing aligned with FDA's New Dietary Ingredient (NDI) guidance, FTC substantiation requirements for health claims, and international market requirements (EU, Canada, Australia). Our regulatory team can advise on testing strategy for specific markets.

Key Tests & Methods

Bioactive ingredient quantification
Identity & authentication
Heavy metals & contaminants
Microbiology & pathogens
Stability & shelf life
Label claim verification

Applicable Standards

FDA 21 CFR Part 101 (food labeling)FDA 21 CFR Part 111 (cGMP)USP dietary supplement standardsEU Novel Food Regulation

Industries We Serve

Functional food brands
Dietary supplement manufacturers
Nutraceutical ingredient suppliers
Wellness product brands
R&D and clinical researchers

How It Works

Three simple steps to your results

01

Submit your samples

Ship samples to our Irvine or San Diego laboratory with your order form.

02

Testing & analysis

Our ISO 17025 accredited scientists run validated test methods.

03

Receive your CoA

Get a signed Certificate of Analysis within 48–72 hours.

FAQ

Frequently Asked Questions

What testing is required for product launch?

Product launch typically requires identity testing, purity analysis, potency verification, and contaminant screening. The exact panel depends on your product type and target market. Qalitex Labs can recommend the appropriate testing scope for your specific product launch needs.

How long does testing take for product launch?

Standard turnaround at Qalitex is 5–7 business days, with rush 48-hour service available for most test types. We recommend planning testing 2–3 weeks ahead of your product launch deadline to allow for any retesting if needed.

Is Qalitex Laboratories ISO 17025 accredited?

Yes. Qalitex Laboratories holds ISO/IEC 17025 accreditation, the international standard for testing and calibration laboratories. This ensures our methods, equipment, and quality systems meet the highest standards of accuracy and reliability.

What is your turnaround time?

Standard turnaround is 5–7 business days. Rush service with 48-hour turnaround is available for most test types. Contact us to discuss your timeline requirements.

What types of products do you test?

Qalitex tests dietary supplements (capsules, powders, gummies, liquids), cosmetics and personal care products, food and beverage items, botanical extracts, and raw materials. We serve brands, contract manufacturers, and Amazon FBA sellers.

How do I submit samples for testing?

Ship your samples to our Irvine or San Diego laboratory with a completed sample submission form. We provide prepaid shipping labels for qualifying orders. Results are delivered electronically via secure portal.

What is nutraceutical testing?

Nutraceutical testing covers the full quality lifecycle of products that bridge food and medicine — including identity and authentication, potency quantification, contaminant screening, microbiology, and stability studies for functional foods and bioactive ingredient products.

Ready to get started?

Request a quote for nutraceutical testing for product launch. Our team responds within 24 hours.