Analysis/Purification

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  • Published date: March 11, 2019
    • Shirley, New York, United States

Impurities and the unwanted by-products, especially the potentially toxic compounds, should be strictly controlled below a certain level set by the regulatory agencies. That’s mainly ascribed to the fact that these pharmaceutical impurities such as residual solvents and degradation substances have a significant role in the purity, safety and quality of the end products. Nonetheless, the analysis and purification of both drug-related and process-related impurities are always challenged by the extensive sources include the starting materials, contaminants, reagents, catalysts, solvents, intermediates, excipients and the leachables and degradation products. Additionally, the impurities are generally presented at very low levels and sometimes in complex sample matrices, which requires more sensitive and specific techniques and approaches to identify and separate them.

On the basis of the network of state-of-the-art laboratories, scientists from BOC Sciences can provide our customers with a comprehensive range of analysis and purification services. With decades of expertise in the testing, inspection, verification and certification for a wide array of industries, our consultants can assist you to conduct a suite of high-quality assessments to address the issues associated with impurity identification and separation. Besides, our highly trained chemists, material scientists, analysts and technicians will work cooperatively to make your customized and innovative analysis services more efficient and timely. In the end, our staff will offer you the collected data which are required to complete relevant risk assessments for meeting the submission requirements.

https://www.bocsci.com/solutions/analysis-purification.htm

Alex Brown
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