Built around the industries we serve. Every testing panel is tailored to your product, market, and regulatory requirements.
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Analytical support for pharmaceutical manufacturers, biotechnology companies, and compounding pharmacies. Potency, purity, sterility, method validation, and product release testing.
Research-grade characterization - purity, identity, sequence confirmation, amino acid analysis, and full release packages for compounders and manufacturers.
Label claim verification, active ingredient quantification, and comprehensive safety testing for supplements and vitamins. Supporting DSHEA compliance and cGMP quality programs.
Analytical testing for botanical products, functional ingredients, adaptogens, and mushrooms. Verify active compounds, support label claims, and ensure product consistency.
of botanical supplement products tested independently fail to match their label claims for active compound content. Third-party accredited testing is your first line of defense.
Comprehensive contaminant screening designed to support USP, FDA, EU Pharmacopoeia, and other international quality standards.
Arsenic, cadmium, lead, mercury + 20 elemental impurities. USP <232>/<233>, EU Pharmacopoeia, and international quality standards.
Total aerobic count, yeast & mold, E. coli, Salmonella, and objectionable organisms. USP <61>/<62>, FDA, and international quality standards.
Screen for methanol, ethanol, acetone, hexane, and other residual solvents. ICH Q3C and USP <467> compliant.
Comprehensive pesticide residue analysis via LC-MS/MS and GC-MS/MS. Supporting global regulatory requirements and quality programs.
Aflatoxins B1, B2, G1, G2 and ochratoxin A for pharmaceutical, nutraceutical, botanical, and functional products. Supporting quality, safety, and compliance programs.
Water activity and moisture analysis for nutraceuticals, botanicals, and finished products. Supporting quality and stability programs.
Streamlined from sample submission to signed certificate of analysis. Built for companies that need accurate results, clear communication, and dependable turnaround times.
Complete our online form, select your panel, and receive chain-of-custody documentation instantly.
Ship to our facility. We accept all matrices - powders, liquids, capsules, plant material, sterile preparations.
Industry-leading scientists utilize validated methods and qualified instrumentation to deliver accurate, defensible results.
Multi-point quality check before release. Every result verified against reference standards and controls.
Digitally signed Certificate of Analysis delivered through our secure portal. QR Code verification. Supporting analytical records available upon request.
Every panel includes a digitally signed COA, secure portal access, and documentation to support defensible scientific results.
| Panel | Category | Key Analytes / Tests | TAT | Tier |
|---|---|---|---|---|
| Pharmaceutical Release | Pharma & Biotech | Identity, Potency, Purity, Impurities | 3-5 Days | Core |
| Sterility & Safety | Pharma & Biotech | Sterility, Endotoxin, Particulates | 14 Days | Advanced |
| Peptide Characterization | Peptides | Identity, Purity, Molecular Weight, Amino Acid Analysis | 5-7 Days | Core |
| Peptide Release | Peptides | Identity, Purity, Moisture, Residual Solvents | 7-10 Days | Advanced |
| Nutraceutical Quality | Nutraceuticals | Label Claim, Potency, Heavy Metals, Stability | 5-10 Days | Core |
| Nutraceutical Safety | Nutraceuticals | Heavy Metals, Microbiology, Mycotoxins | 10-14 Days | Advanced |
| Botanical Active Profile | Botanicals | Active Compounds, Marker Compounds, Identity | 5-7 Days | Core |
| Botanical Safety | Botanicals | Heavy Metals, Microbiology, Mycotoxins, Pesticides | 10-14 Days | Advanced |
Answers to the questions we hear most about our testing, accreditation, turnaround, and submission process.
We support pharmaceutical, biotechnology, peptide, nutraceutical, botanical, and functional ingredient manufacturers with analytical testing, characterization, safety screening, and quality assurance services.
Yes. Modern Analytical Sciences operates under an ISO/IEC 17025:2017 accredited quality management system with validated methods, calibrated instrumentation, and documented quality controls.
Most analyses are completed within 5-10 business days, with many services available on expedited timelines. Turnaround time varies by test panel and sample complexity.
Yes. Rush testing is available for many analyses. Contact our team for availability and estimated turnaround times.
Yes. Our scientific team routinely develops and validates custom methods for novel ingredients, proprietary extracts, and emerging compounds. Development timelines vary based on complexity and reference standard availability.
Both. We test raw materials, extracts, in-process materials, active ingredients, and finished products across a wide range of industries and product categories.
Available panels include heavy metals, microbiology, mycotoxins, pesticide residues, residual solvents, moisture, water activity, and other product-specific contaminants.
Yes. All completed testing includes a digitally signed Certificate of Analysis accessible through our secure client portal.
Yes. Our scientific and quality teams can help identify appropriate testing based on your product type, ingredients, specifications, and quality objectives.
Yes. Our testing programs are commonly used by manufacturers operating under cGMP, supplier qualification, product release, stability, and quality assurance programs.
We support testing for kava, kanna, kratom, functional mushrooms, adaptogens, polyphenols, and other botanical ingredients, extracts, and finished products.
Peptide testing services include purity analysis, identity confirmation, sequence verification, amino acid analysis, heavy metals, residual solvents, moisture determination, and stability studies.
Yes. We support dietary supplements, vitamins, minerals, amino acids, protein powders, herbal products, probiotics, functional ingredients, and finished nutraceutical formulations.
Absolutely. Our scientific and quality teams are available to discuss testing methodologies, specifications, results, and technical questions.
Complete a Chain of Custody form, ship or deliver your samples to our laboratory, and our team will confirm receipt and testing requirements before analysis begins.
Contact us. We regularly work with novel ingredients, proprietary formulations, and emerging compounds and can discuss custom testing solutions tailored to your needs.
Standard results in 5-7 business days. Rush processing available in 24-72 hours.