A comprehensive quality assurance programme at every stage of procurement, manufacture, packing & distribution ensure that products not only meet but also surpass pharmacopoeial requirements. Stringent control systems & procedures ensure compliance with CGMP standards.

Our Quality assurance deptt. comprise of a seperate department IPQA which monitors inprocess controls to assure inbuilt quality in the product.



We ensure the quality of starting and packaging materials by following Specifications & Standard Test Procedures. Our Quality control deptt. is responsible for all sampling & analysis work related to raw material, in -process and finished goods validation samples & stability samples and aim at carrying out all requirements of current Good Laboratory Practices (cGLPs). We ensure that the incoming, in-process and final inspection is done as per documented procedures.


R & D in Medicamen is a committed endeavour & spans several disciplines including organic chemistry, biopharmaceutics, pharmacology, microbiology etc. The aim is to provide effective yet safe formulations with superior organoleptic properties for better customer acceptability. The R & D wing is equipped with new generation instrumentation ranging from U.V. spectrophotometer to HPLC., IR etc.


Medicamen’s endless pursuit for quality pharmaceuticals has given it an edge over others to access the global market. The Group entered the Export market in 1996 & since then has fast emerged on the international arena as one of the major exporters of finished formulations.


© Medicamen Biotech Limited. All Rights Reserved.

website designed & developed by Blue Moon Technologies.