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Validation GlobeTech strives to improve quality in manufacturing companies that implement a GMP (Good Manufacturing Practice), GDP (Good Distribution Practice) and GLP (Good Laboratories Practice) such as Pharmaceuticals, Hospitals, Laboratories, etc. by offering professional validation services. Wide range of validation such as but not limited to: - DQ,IQ,OQ,PQ (qualification) n- facility validation n- HVAC validation n- production, monitoring and laboratory instruments & equipment n- safety equipment n- bio-safety cabinets n- HEPA integrity n- clean room classification n- storage and transportation n- cold chain, etc Poor validation, result in an inefficient system, which can cause long-term problems and prove costly. Overall, GlobeTech is characterized as a dependable resource, which seeks to be identified not only a "member", but also an "asset" to anyone's project team. In accordance with the validation plan, validation reports and protocols are prepared to document specific decisions, actions and their resultant effect on meeting the design intent. Systems are tested, test results are analysed, and performance validated to demonstrate that systems perform according to the design intent under a variety of conditions. The validation report is the primary record document for validating each system and equipment. |
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