Pharmaceutical Raw Material Articles & Analysis
3 articles found
Solid-liquid separation is necessary in many industries for compliance, quality control, and efficient production processes. In the pharmaceutical industry, solid-liquid separation is conducted in applications such as biocatalysis, active pharmaceutical ingredient (API) purification, and chromatography, to name a few. ...
However, in principle, the newly added medicinal excipients must first apply for NDA (New Drug Approval) test and establish relevant quality standards, and secondly, they must be generally recognized as safe substances, namely GRAS-grade raw materials; otherwise, they cannot be approved for use as a pharmaceutical excipient. ...
There are STANDARD Guidelines used to define the Identification and Purity of compounds used in Pharmaceutical and Cosmetic formulations, as well as the final Products. These protocols are described in great detail in the various Monographs of the United States and British Pharmacopoeias, the National Formulary (USP/NF and BP), the International FAO/WHO Codex (CODEX) and other Regulatory ...