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Elemental Impurities by ICP-MS

Comprehensive elemental analysis for accepted pharmaceutical materials, products, and matrices.

Elemental Analysis

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.

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Elemental Impurity Testing by ICP-MS

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.

01

Product Details

Product or material name, grade, matrix, and dosage form.

02

Specifications

Applicable specification and required elemental panel.

03

Target Limits

Target limits and regulatory market requirements.

04

Methodology

Current method, validation, verification, or prior laboratory information.

05

Logistics & Safety

Sample quantity, standards, safety information, and target date.

TS
Evaluation

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.

  • Approved elemental panel & methodology
  • Preparation procedures and analytical results
  • Applicable limits, observations, and deviations
  • Final quality review and clear conclusions
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Get in touch with our experts to discuss your pharmaceutical analytical testing needs and ensure absolute compliance and quality.