Completion year: 2014
We at Ipram International started with manufacturing of injectables topical and dry suspension powders in year 2004. We started with Injectables manufacturing right from the very beginning. Not only cGMP, GLP, GSP is followed strictly in respect of production of all categories of drugs, but validation of all equipment’s, machines, instruments and analytical procedure is also done regularly. Because of delicate and critical nature parenteral products are sterile and pyrogen free. Quality is built into them during each step of manufacturing The sterile area has been specially designed and provided with HVAC system using HEPA filters, laminar flow hoods, approved deionized, R.O and distilled water system. Decartoning, washing, nonsterile area, sterile formulations, filtration, sterilization, filling, stoppering cum sealing and gowning facilities are isolated from each other and fitted with necessary control Instruments. The quality is built right from the procurement of raw material up to filling into final containers and packaging.
In Q.C lab we have microbiology section and LAL test is also performed to exclude any pyrogen from the injectables. There are separate instrumentation and analytical facilities, and validation of analytical procedures are also done regularly. All the procedures are carried and supervised by highly qualified and experienced scientists. We excel with quality and aim at healing the ailing humanity with quality medicines of highest standard. We pray Allah Almighty to help us in achieving our noble goals.