Any pharmaceutical product manufacturer, requires a quality control which is one of the foremost requisite with regard to regulatory compliances. A significant portion of the cGMP regulations (21 CFR PART 211) and all pharmacopeia methods such as USP, IP, EP, JP, BP and In-house methods pertain to the quality control testing of products. Shiva provides expert analytical services in all areas of testing from raw materials, excipients, APIs, Bulk drugs, intermediates to finished products. Shiva's sophisticated pharmaceutical testing lab operates as an extension of your QC and Analytical R&D laboratories.