The QC department comprises of highly skilled and experienced professionals using sophisticated testing procedures for the testing of active pharmaceutical ingredients, excipients, packaging components and finished pharmaceutical dosage forms are carried out as per latest pharmacopoeial standards. We have the evaluation and approval system for different suppliers at our Quality Control Laboratory.
Retaining Samples of Finish Products
Other than Routine testing, QC also has samples retaining room (for legal reference).Samples from each batch are kept over there for legal reference and as a record for stability studies which is being carried out according to the written standard procedures. The samples of finished items are retained up to one year after expiry as of the ministry of health to ensure the shelf life of the product. Retaining samples are very much helpful to any investigator against the product complaint.Other than Routine testing, QC also has samples retaining room (for legal reference).Samples from each batch are kept over there for legal reference and as a record for stability studies which is being carried out according to the written standard procedures. The samples of finished items are retained up to one year after expiry as of the ministry of health to ensure the shelf life of the product. Retaining samples are very much helpful to any investigator against the product complaint.
Caliberation Programme
Calibration is a set of operations that establish, under specified conditions the relationship between values of quantities indicated by a measuring instrument (or values represented by a material measure) and the corresponding values realized by standards. Here in global pharmaceuticals, we have a periodic Calibration program for all the equipments/instruments. Calibration are being done internally and some times through external parties along with traceability as per standards.
Microbiology Laboratory
Microbiology laboratory is the vital part of pharmaceutical industry in the modern era. Testing of sterile as well as Non-sterile dosage forms as per standard procedures is inevitable so that contamination free products to be supplied to the end user. In Global Pharmaceuticals, we have well furnished micro laboratory with highly skilled professionals duly equipped with state of the art instruments for the various microbiological testing of sterile products, Area monitoring, water testing and LAL (Litmus Amoebocyte Lysate) for Pyrogen testing. Sterility testing of the finished products is performed to ensure the sterility of the parenteral products prior to their delivery to the market.
