Conducting elemental impurity testing of raw materials, active pharmaceutical ingredients, intermediates, and formulations based on ICH-Q3D guidelines/JP18.
Our company is capable of conducting screening analysis of elemental impurities based on the ICH-Q3D guidelines, as well as the development, validation, and testing of quantitative methods or limit test methods, using analytical instruments managed in compliance with GMP regulations. 【Features】 ■ Development, validation, and testing based on years of proven experience, ensuring optimal testing methods ■ High sensitivity and reliability in analysis using GMP-compliant ICP-MS For more detailed information, please refer to the "Related Links."
Inquire About This Product
basic information
If you have any questions or inquiries, please feel free to contact us through the "Contact Us" section on this page or via the "Contact Form" on our official website.
Price range
Delivery Time
Applications/Examples of results
For more details, please contact us.
Company information
We are a contract analysis laboratory (Kyoto) that complies with pharmaceutical GMP standards, part of the Eurofins Group, which operates a global contract analysis business. We efficiently and swiftly respond to various testing needs from the early stages of product development to commercialization, while adhering to various regulations. Please feel free to contact us if you have any requests.
