PharmaChem believes in being more than a catalyst. Apart from our core competency in sourcing APIÕs and generic pharmaceutical we design the process, scale up the process with environmental safety consideration. Further we conduct studies on identification and quantification of impurities, perform stability study of drugs, validation of analytical methodologies, implementing cGMP practices, preparation of COS (certificate of suitability)/DMF files. We can take up contractual agreements for conducting bio-availability studies and bio-equivalent studies.

We also specialise in offering clients our bonded warehousing facility in Europe. In a nutshell, PharmaChem is not another representative office, but functions as your own strategic business unit.