Quality

The Quality Control Culture

The Research Culture

 
The important aspect of pharmaceutical manufacturing requires detailed documentation and auditing through ‘Total Quality Management’.  Here at ‘ALVES’ every single step of the manufacturing process, starting from the acquisition of raw materials, is fully documented and continuously audited to ensure that all protocols established are duly validated. These measures assure that high quality of pharmaceutical products are manufactured and distributed so as to meet its shelf life to internationally accepted standards of quality, purity, efficacy and safety.

The facility has a full-fledged Chemical, Instrumentation; Microbiology & Sterility Laboratories provided with Class 10000 environment and SS horizontal Laminar Air Flow Units. The full spectrum of microbiological and sterility validation tests are conducted for on-going constant microbiological monitoring of all processes and products, as well as personnel and production areas, to ensure total product purity.

The Quality Assurance Department managed by qualified and experienced personnel and equipped with advanced analytical equipment lays emphasis on:-

  • Regular validation of Products, Processes and Test Methods
  • Regular calibration of all instruments, to guarantee product output of consistent top quality
  • Regular quality audit and validation by external agencies
  • Regular monitoring approval of vendors based on stringent procedures laid down
  • Regular up gradation of the analytical facilities
  • Regular up gradation of manufacturing facilities to meet latest GMP requirements
  • Regular training to improve the professional skills of personnel
 
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