Quality Control

Quality A&C

Testing & Quality Control

Quality Assurance

ISO9001: QMS

cGMP

Quality Policy

Quality Control & Testing

CIRIN's philosophy has always been based on certain principles in order to satisfy customer needs. We believe on RELIABILITY, QUALITY, CONTINUITY and CONSISTENCY. The quality policy of CIRIN fully depicts our commitment:

"CIRIN PLEDGES QUALITY"

We understand the term quality as being a sum of reliability, the continuity of supply, excellence in processing, consistent analytical control and prompt customer service. It also involves well documented testing methods under GMP conditions fulfilling American and European pharmacopial international standards. These are certificates of analysis which are essential to provide necessary documents in support thereof; thus enabling our customers to rely on our products.

There are two sections working under Quality Control Department i.e. Chemical Section and Microbiological Section. Quality Control Department is very spacious with all latest sophisticated equipments i.e. HPLC (Shimadzu, Japan), gradient and isocratic both, UV-VIS Spectrophotometer (Genesis, USA), Karl Fisher (Orion, Switzerland), Analytical balances (Sartorius, Germany and AND), Dissolution Apparatus (Electrolab India), Polarimeter (China), Oven (Mammert, Germany), Melting Point Apparatus (Gallenkemp, UK), Water Bath (China), Muffle Furnace (Thrmolyn, USA), Hardness Tester (Indian) Disintegration Apparatus (Indian), Friabilitor (Pakistan), Climate chamber for stability purpose, (China), LOD apparatus (China), Flame Photometer (Genway UK ), Ultrasonic bath (ELMA, USA), pH meter (Orion, Thermo), Autoclaves (Pakistan), Cool incubators (China), Hot incubators (Mammert Germany), Microscope (China), Vortex Mixer (China), Tube incubator (China) for BET, Laser Particle Counter (China), Air sampler (China) and many other basic equipments used in laboratory. In all we are fully equipped to meet all basic as well as advance requirements in all kind of testing.

We are ISO 9001-2000 Certified and implementing this system in true sense. We have validated most of our Analytical Methods and manufacturing processes and still working on validations as it is a basic requirement of GMP. We also have a stability program in which regular and post market stability studies are conducted. We have HPLC gradient and Isocratic both system, which is considered a backbone of quality control in any pharmaceuticals industry and one of the latest technique for the analysis of Pharmaceutical products.

Moreover qualification and Calibration of all the equipments is being regularly carried out by internal and external approved sources.

Quality of Human Resource in QC & Testing