Pharmaceutical Analytical Testing
Comprehensive chemical and instrumental testing across accepted stages of the product lifecycle.
Pharmaceutical Analytical Testing
Globyz Clinical Solutions supports pharmaceutical manufacturers, importers, distributors, virtual companies, and product developers with chemical and instrumental testing across accepted stages of the product lifecycle. Each project is governed by an approved scope, suitable method, qualified equipment, trained personnel, controlled records, and agreed reporting requirements.
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Quality Guaranteed
Highest analytical standards
Testing Scope
Globyz Clinical Solutions provides analytical testing for active pharmaceutical ingredients, raw materials, excipients, finished pharmaceutical products, natural health products and cosmetics. Our services cover identity, assay or potency, purity, related substances, degradation products, residual solvents, elemental impurities, water or moisture content, pH and other physicochemical quality attributes.
Finished-product testing also includes dosage-unit uniformity, dissolution, disintegration and product-performance testing. Natural health product and cosmetic testing includes the identification and quantification of active or marker ingredients, evaluation of physicochemical properties and testing for relevant impurities and contaminants.
Supporting Key Decisions
These services support material qualification, product development, batch release, investigations and regulatory compliance. Controlled analytical procedures, scientific data review and clear reporting provide reliable evidence for product-quality assessment and informed manufacturing and quality decisions.
Technical Acceptance
A rigorous review process ensures absolute clarity and capability before any work commences.
The laboratory reviews the specification, method version, product matrix, acceptance criteria, sample quantity, standards, reagents, columns, instrument configuration, system suitability, software, calculations, data processing, and reporting needs before accepting work.
Controlled Execution
Testing is scheduled only after scope approval and readiness confirmation. Samples, standards, solutions, instruments, calculations, observations, deviations, and review activities are meticulously documented under applicable procedures to ensure complete traceability and compliance.
Comprehensive Reporting
The final deliverable may be a certificate of analysis, analytical report, method transfer or validation report, investigation report, or another agreed controlled record.
Accelerate Your Analytical Testing
Get in touch with our experts to discuss your pharmaceutical analytical testing needs and ensure absolute compliance and quality.