Elemental Impurities by ICP-MS
Comprehensive elemental analysis for accepted pharmaceutical materials, products, and matrices.
Elemental Impurity Testing by ICP-MS
Globyz Clinical Solutions provides ICP-MS based elemental analysis for accepted pharmaceutical materials, products, and health product matrices. Testing is accepted after review of the required elemental panel, specification, method, sample preparation, digestion needs, target limits, standards, interference controls, equipment readiness, and reporting requirements.
Request an Elemental Impurity Review
Precision Testing
Advanced ICP-MS technology
Required Project Information
To ensure accurate and compliant testing, we review the following critical information before initiating any project.
Product Details
Product or material name, grade, matrix, and dosage form.
Specifications
Applicable specification and required elemental panel.
Target Limits
Target limits and regulatory market requirements.
Methodology
Current method, validation, verification, or prior laboratory information.
Logistics & Safety
Sample quantity, standards, safety information, and target date.
Technical Suitability
The review considers sample preparation, digestion or dilution approach, calibration strategy, internal standards, blanks, interference control, detection capability, carryover, recovery, precision, and system suitability.
Method Readiness
A client or compendial method may require transfer, verification, or additional suitability work before routine use. The required scope is documented and agreed before testing begins.
Comprehensive Reporting
The controlled report identifies all critical components of the analysis to ensure complete transparency and regulatory compliance.
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Approved elemental panel & methodology
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Preparation procedures and analytical results
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Applicable limits, observations, and deviations
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Final quality review and clear conclusions
Accelerate Your Analytical Testing
Get in touch with our experts to discuss your pharmaceutical analytical testing needs and ensure absolute compliance and quality.