2021-08-26 06:42 The method of purity studies, impurities identification and characterization, stability studies are important step in drug development, these methods mentioned above are widely used in quantitative and qualitative analysis of drugs. The mastery of th ... дальше
2021-08-25 13:47 Standards and reagents are usually one of key elements in achieving the best performance and compliance of analytical instruments and their reliability is of prime importance.
2021-07-21 10:53 To ensure the healthy growth of the pharmaceutical market, while encouraging innovation and research, the US Food and Drug Administration (FDA) has developed a series of comprehensive measures and management tools. In IND application or NDA submissio ... дальше
2021-06-27 20:40 To ensure the healthy growth of the pharmaceutical market, while encouraging innovation and research, the US Food and Drug Administration (FDA) has developed a series of comprehensive measures and management tools. In IND application or NDA submissio ... дальше
2021-06-27 20:26 BOC Sciences provides general analysis and purification services for the clients from candidates discovering to clinical trial chemicals. Related date is provided by our analytical team throughout the development process. Our cGMP analytical laborato ... дальше
2021-05-19 11:04 Method validation is essential for compliance with current good manufacturing specifications (CGMP) and good laboratory specifications (GLP). Analytical method validation (AMV) is the requirement of the biopharmaceutical industry for all methods used ... дальше
2021-03-19 07:43 The successful development of pharmaceutical products depends on its effectiveness and safety. In the process of pharmaceutical development and production, the physical and chemical properties, the impurities introduced in the production process,
