We are committed to manufacture the packaging materials of right quality at right time to the customer satisfaction. We endeavor to continually improve the quality management systems to delight customers by providing assurance on product quality.
M. Madan Mohan Reddy
All manufacturing facilities and our policies and procedures are governed by current Good Manufacturing Practices(cGMPs). These are formally audited regularly during the year and all issues that may arise are closed out through corrective and preventive action measures (CAPA).
The documentation that is available with us is in line with cGMP requirements as applicable in Pharmaceutical industry and has been audited and certified by several leading finished formulation pharmaceutical companies.
All our personnel are thoroughly trained on various aspects of cGMP on a continuous basis to make them constantly aware of cGMP requirements and update if needed.
Our Drug Master File, maintained with the FDA in USA contains all product specifications, quality requirements, product drawings, USP test results and all other relevant technical information.
We were ISO 9001 certified in year 2006 and have a DMF with US FDA since 2006. We also have certified as DS/EN ISO: 15378: Primary Packaging Materials for Medicinal Products.
We have been audited and approved by several domestic and international pharmaceutical companies. Many of them have awarded us "Approved Vendor" status in recognition of our facility as per cGMP norms, product quality and reliable services.
All drug containers manufactured by us are in compliance with standards set by the United States Pharmacopoeia, section <661>. Additionally, we have on file USP <661> test results for more than 50 different bottles as filed in our DMF.