About Us

We have initiated Pharmacrony consulting with a objective to add values in Regulatory Operations of Pharma manufacturing units.Our CEO had been in the industry with last 27 years and was instrumental in successfully achieving USFDA/MHRA/ TGA/WHO-Geneva and other regulatory accreditations ,upgradation of plants , projects ,Implementation of QMS, Operational excellence and people development on different levels and he has a track record of one of excellent technocrat in Industry.

Success of any regulatory site is based on how they investigates their deficiencies and how do they address it transparently. This lacuna in defining correct way of investigations is just eating up Organisations. We have expertise to investigate and to train technical team on all aspects on QMS. We ensures a well defined and logical way to conclude your deviations , Market complaint investigations , OOS/OOT investigations and all your GxP documents.

Designing future starts with designing of site layout and foundation of QMS system .We understands logical flow and we believe that design of site is the starting point to make it compliance easy site. Our expertise on plant design will take care of all regulatory queries in future for your site. Or expertise in establishing QMS gives a better prospects on the front of regulatory compliance.

We understand the base for creating success on the professional front. We know all factors which leads for a successful carrier in Pharma Domain. We train our clients on carrier path and we prepare them not only on academics or on Guidelines but on other soft skills like emotional intelligence and Psychological behaviors as well . Our objective is to create best techno commercial human being to serve the Pharma Industry.