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Included With All Manufacturing

Quality Testing Included With Every Order

Every product we manufacture includes comprehensive third-party testing through our network of ISO 17025 accredited laboratories. Safety testing, potency verification, and COA generation are all part of our service.

Testing for Nutricraft Manufacturing Clients Only

Quality testing is included as part of our manufacturing services. We do not offer standalone testing for products manufactured elsewhere. Looking for your own lab? We recommend Eurofins or NSF.

7-10
Days Standard Testing
0 %
FDA Compliance
5+
Partner Labs
ISO
17025 Certified
Laboratory technician conducting quality testing on supplement products with scientific equipment

Testing Included With Every Batch

Every manufacturing order includes comprehensive testing through our ISO 17025 accredited lab partners

Identity & Purity Testing

  • Raw material identification
  • Active ingredient verification
  • Botanical authentication
  • Adulterant screening

Ensures you're getting exactly what you ordered

Microbial Testing

  • Total plate count
  • Yeast and mold
  • E. coli and Salmonella
  • Staphylococcus aureus

Protects consumers from harmful pathogens

Heavy Metals Testing

  • Lead (Pb)
  • Arsenic (As)
  • Cadmium (Cd)
  • Mercury (Hg)

Meets regulatory limits for toxic elements

Potency & Label Claims

  • Active ingredient assay
  • Vitamin/mineral content
  • Dissolution testing
  • Homogeneity verification

Validates your label claims are accurate

Stability Testing

  • Accelerated stability
  • Real-time stability
  • Photo-stability
  • Freeze-thaw cycles

Determines shelf life and storage conditions

Physical Testing

  • Tablet hardness
  • Disintegration time
  • Moisture content
  • Particle size distribution

Ensures product consistency and performance

Pesticide & Residue Testing

  • Multi-residue pesticide screening
  • Herbicide detection
  • Fungicide analysis
  • Glyphosate testing

Critical for botanical ingredients and organic claims

Allergen Testing

  • Big 9 allergen panel
  • Gluten testing (for GF claims)
  • Cross-contamination screening
  • Soy and dairy detection

Protects allergic consumers and validates label claims

Our Testing Process

Streamlined testing workflow with full traceability and documentation

1

Sample Collection

Day 1

Proper sampling from production batches following cGMP protocols

2

Lab Coordination

Day 2

Samples sent to ISO 17025 certified third-party laboratories

3

Testing Execution

Days 3-7

Comprehensive testing according to USP, FCC, or custom specifications

4

Results Review

Day 8

Technical review of all test results against specifications

5

COA Generation

Day 9

Certificate of Analysis prepared with full traceability

6

Quality Release

Day 10

Final quality approval and product release for distribution

Global Compliance Standards

Testing protocols tailored to meet regulatory requirements worldwide

UN United States

Standards

FDA cGMP USP Standards NSF Certified FDA NDI Requirements

Key Testing

Heavy metals, microbials, identity, potency

CA Canada

Standards

Health Canada GMP NPN Requirements NHPD Standards Site License

Key Testing

Bilingual labeling, contaminants, stability

EU European Union

Standards

EU GMP EFSA Guidelines Novel Foods ISO 22000

Key Testing

PAH, mycotoxins, pesticides, allergens

AU Australia

Standards

TGA Listed AUSTL Requirements PIC/S GMP FSANZ Standards

Key Testing

Therapeutic claims validation, bioavailability

California Prop 65 Compliance Testing

Required testing for supplements sold in California with strict Safe Harbor limits

Selling in California? Prop 65 Testing is Mandatory

California Proposition 65 requires warnings on products containing certain levels of heavy metals and chemicals. Testing is required to determine compliance and avoid penalties up to $2,500 per violation per day.

Safe Harbor Limits (Daily Dose)

Lead (Reproductive) 0.5 mcg/day
Arsenic (Inorganic) 10 mcg/day
Cadmium 4.1 mcg/day
Mercury 0.3 mcg/day

What We Test

  • ICP-MS heavy metal analysis at parts-per-billion sensitivity
  • Daily dose calculations based on label directions
  • Compliance report with warning recommendations
  • Label language guidance if warnings required

Important Note

Even if you're not based in California, you must comply with Prop 65 if you ship products to California customers. This applies to online sales through Amazon, your website, or any distribution channel. Testing typically takes 7-10 business days.

Lab Certifications & Accreditations

ISO 17025

Lab accreditation standard

cGMP Compliant

Current Good Manufacturing Practices

FDA Registered

All partner labs FDA-registered

Health Canada

Licensed for Canadian market

USP Verified

United States Pharmacopeia standards

NSF Certified

Third-party certification available

Ready to Launch Your Product?

All manufacturing orders include comprehensive quality testing, COA generation, and regulatory compliance verification.

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Frequently Asked Questions

Common questions about quality testing included with our manufacturing services