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VAQ Strategies has experience with qualification and change control managment of Water Spray Sterilization Technology (Water-Spray, Saturated Steam, Steam-in-Place, Dry Heat, Vaporized Hydrogen Peroxide), Bioburden Reduction Equipment (Commodity and Container Processing), Computer Systems (Allen Bradley HMIs and PLCs,Cognex Vision Systems, Wonderware HMI/SCADA and Data Historan), Utilities (Pharmaeutical Water Systems, Compressed Gases, HQS, Plant Steam, Distillation Systems) within GxP environments. We offer support of the entire Validation Life Cycle along with devolepment studies.
We offer comprehensive services including but not limited to the generation and approval of Validation Documentation (IO/OQ/PQ protocols),Quality Investigations (OOS, Stability Failures, Equipment Excursions), Product Complaints (medical devices 21 CFR Part 820 and finished pharmaceutical products 21 CFR Part 211), Risk Management and Data Integrity Support, along with technical documentation support (Creation and Updates of procedures, specifications, URS, design decouments, Trace Matrices, Validation Plans).
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