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.
- Company：メルク株式会社ライフサイエンス（シグマ アルドリッチ ジャパン合同会社）
- Price：Other
