製藥產業 Pharmaceutical:

A comprehensive range of Media, conforming specifications of pharmacopoeia guidelines is available with HiMedia for complete testing methods in pharmaceutical laboratories. With the harmonization of USP/EP/BP/JP/IP, newer testing protocols have to be implemented for testing of non-sterile drug products. This also includes changes in composition of culture media used to test these products for specified organisms. To meet the consistency in microbiological testing methods, HiMedia has formulated the dehydrated culture media in accordance with the harmonized methods. They are designed to meet the latest harmonized USP . It covers Antibiotics Assay medium, Sterility Testing media, Microbial Limit Test - Harmonized media, Vitamin Assay media and Neutralizing media. Testing of these medias as per new testing guidelines is carried out by validated methods in quality control department. The goal of global pharmacopoeias harmonization is to promote the acceptance of consistency and uniformity of microbiology methods used by companies throughout the world.
HiMedia提供全面的媒體,符合藥典指南的規範,可用於製藥實驗室的完整測試方法。隨著USP / EP / BP / JP / IP的協調,必須實施更新的測試方案以測試非無菌藥物產品。這還包括用於測試特定生物體的這些產品的培養基組成的變化。為了滿足微生物檢測方法的一致性,HiMedia按照統一的方法配製了脫水培養基。它們旨在滿足最新的協調USP 。它涵蓋了抗生素檢測培養基,無菌檢測培養基,微生物限度檢測 - 協調培養基,維生素檢測培養基和中和培養基。根據新的測試指南對這些媒體的測試通過質量控制部門的驗證方法進行。全球藥典協調的目標是促進全世界公司使用的微生物學方法的一致性和一致性的接受。