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ISO 17025 Accredited

Stability Testing for Dietary supplements — Expert Lab Services

Expert stability testing tailored for dietary supplements brands. Regulatory-compliant testing with COA documentation for product safety and market access.

ISO 17025 Accredited 48-Hour Turnaround Available 500+ Test Methods FDA-Compliant Reporting Dual Locations: Irvine & San Diego, CA
ISO 17025 Accredited ISO 17025
48-Hour Rapid Testing 48h Turnaround
Satisfaction Guaranteed 100% Satisfaction

Quick Answer

Stability Testing for dietary supplements involves analyzing product samples using validated scientific methods to verify safety, purity, potency, and regulatory compliance. Accredited labs like Qalitex use instrumentation such as HPLC, ICP-MS, and microbiology assays to generate Certificates of Analysis (COA) required by FDA, Amazon, and retail partners.

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Dietary supplements brands require specialized testing to ensure product safety, regulatory compliance, and consumer trust. Qalitex Laboratories provides stability testing specifically designed for the dietary supplements industry. Qalitex Laboratories specializes in dietary supplement stability testing that ensures your products remain safe, potent, and effective throughout their intended shelf life. Our testing services comply with FDA regulations, follow GMP standards, and support your product's market longevity. Our testing protocols are calibrated to the unique requirements of dietary supplements products, from raw material verification to finished goods release testing.

Stability Testing Tailored for Dietary supplements

The dietary supplements industry has specific testing requirements driven by FDA regulations, marketplace compliance (Amazon, retail), and consumer safety expectations. Qalitex designs testing panels specifically for dietary supplements products, ensuring you meet all applicable standards while optimizing your testing budget. Our scientists understand the unique matrices and formulation challenges of dietary supplements products.

What Is Stability Testing and Why It Matters

Stability testing evaluates how a dietary supplement performs under various environmental conditions — temperature, humidity, and light. We conduct both real-time and accelerated stability studies per ICH Q1A(R2) guidelines, assessing active ingredient potency, microbiological integrity, packaging durability, and organoleptic properties (color, odor, texture).

Shelf Life Testing

Shelf life testing defines how long a supplement remains both safe and effective, providing the data needed for accurate expiration dating. We simulate extended storage under real and accelerated conditions, testing at 0, 1, 3, 6, and 12 months, evaluating degradation of actives and risk of microbial growth.

Our Testing Process

We test a wide range of formats: tablets, capsules, softgels, powders, gummies, and liquids. Every study includes a protocol design phase, appropriate chamber conditions (ICH Zone I–IV), testing intervals, and a final stability report with CoA documentation suitable for FDA submission.

Key Tests & Methods

Real-time stability studies
Accelerated stability (ICH Q1 conditions)
Potency & label claim over time
Microbial integrity testing
Packaging compatibility
Organoleptic evaluation

Applicable Standards

ICH Q1A(R2)FDA Guidance for stability testingUSP dietary supplement standardscGMP 21 CFR Part 111

Industries We Serve

Dietary supplements (all formats)
Nutraceuticals
Functional foods
Amazon FBA products requiring expiry dating
Contract manufacturers

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 stability testing do dietary supplements brands need?

Dietary supplements brands typically require identity testing, purity analysis, contaminant screening (heavy metals, pesticides, microbiology), and potency verification. Specific requirements depend on the product type, target market, and applicable regulations (FDA, FTC, state laws).

Do you provide COA reports for dietary supplements products?

Yes. Every test at Qalitex generates a detailed Certificate of Analysis (COA) that includes test methods, results, specifications, and pass/fail determinations. Our COAs are accepted by FDA, Amazon, retailers, and international regulatory bodies.

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 the difference between real-time and accelerated stability testing?

Real-time stability testing stores products under normal conditions and tests at intervals over months or years, while accelerated stability testing uses elevated temperature and humidity to predict shelf life faster. Qalitex performs both types per ICH Q1A(R2) guidelines.

Ready to get started?

Request a quote for stability testing supplements for dietary supplements. Our team responds within 24 hours.

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