The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for the quality assurance of medicines. Standards are developed by the Committee through worldwide consultation and an international consensus-building process. The following new guidelines were adopted and recommended for use: procedure for adoption of ...

The aim of the research is to study the working capital management in the area of pharmaceutical industry. Since the study is associated with the pharmaceutical sector of India, the main reason to choose this sector for the research is that in the case of pharmaceutical firms, the market leadership is not based on product innovation, rather on new product development. Thus these firms of pharma...

Sterility test is an established method for detecting the presence of viable forms of microorganisms in or on finished pharmaceutical products. Sterility, in this sense, means that a product is free from viable microorganisms (although not necessarily metabolic by-products or toxins). The classic form sterility test examines a pharmaceutical product in contact a culture medium, as a way of dete...

Abstract: Background: Intellectual property rights (IPR) are described as concepts, creations, especially artistic endeavors around which the community is ready to confer position of ownership. There various sorts intellectual protection such patents, copyright, trademarks, and so on. A patent an acknowledgment innovation that meets standards worldwide uniqueness, non-obviousness, well commerci...