Certified Reference Material (CRM) for Elemental Impurity Analysis of Pharmaceuticals
Manufactured in facilities accredited to ISO/IEC 17025 and ISO 17034 according to the ICH Q3D guidelines.
The "Certified Reference Material (CRM) for Elemental Impurity Analysis of Pharmaceuticals" is a mixed solution prepared at concentrations that correspond to the permissible daily exposure (PDE) values outlined in the ICH Q3D guidelines. It ensures the safety of your pharmaceuticals by adhering to the elemental concentration limits for oral, non-oral, and inhalation routes. With the elimination of human preparation errors, it allows for more accurate analysis and reproducibility. 【Features】 ■ Manufactured in facilities accredited to ISO/IEC 17025 and ISO 17034 ■ Improved stability through innovative container design ■ Pre-prepared mixed solution *For more details, please refer to the PDF document or feel free to contact us.
basic information
【Other Features】 ■ Traceable to at least two references (NIST, BAM) ■ Information on appropriate uncertainty, expiration dates, and storage ■ Comprehensive documentation in accordance with ISO Guide 31 ■ Ensures reliability through the use of certified reference materials ■ Utilizes special fluoropolymer bottles ■ Enhances stability by sealing in a highly airtight aluminum bag ■ Significantly reduces preparation time and costs ■ Eliminates human preparation errors for more accurate analysis and reproducibility *For more details, please refer to the PDF document or feel free to contact us.
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For more details, please refer to the PDF document or feel free to contact us.
