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Friday, 08 May 2009 06:35 |
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Our production facility is operated under the strict governance of quality control standards which meet or exceed those required by governmental oversight. The facility itself is divided into many areas, each serving a specific purpose. They are loosely categorized into two identifiable groupings: storage and production. General Facility Organization The storage facility is utilized at several points during the production process, serving as: Bulk ingredient and materials storage and quarantineBulk product storage and quarantine (of finished, but not yet packaged tablets)Finished product quarantine storage (pending final testing and approval), andFinished, market-ready product storage The production facility is also further divided into two general productions lines: Oral pharmaceutical productionOral pharmaceutical packagingInjectable pharmaceutical productionInjectable container sterilizationInjectable pharmaceutical packaging We are in the process of expanding the pharmaceutical production facility to double the production capacity for all product lines. The Production Process Generally speaking, the production of sterile pharmaceuticals is a six stage process: Acquisition and acceptance of bulk raw materialsPre-production preparation and planningPharmaceutical component manufacturingPharmaceutical component packagingPost-production storage and testingDelivery of finished product to distribution network
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