Our Services
Validation Support
VAQ Strategies is skilled in qualification and change control for Sterilization Technology—including Water-Spray, Saturated Steam, Steam-in-Place, Dry Heat, and Vaporized Hydrogen Peroxide—as well as Bioburden Reduction Equipment for both commodity and container processing. Our expertise extends to Computer Systems (such as Allen Bradley HMIs and PLCs, Cognex Vision Systems, Wonderware HMI/SCADA, and Data Historian) and Utilities (including Pharmaceutical Water Systems, Compressed Gases, HQS, Plant Steam, and Distillation Systems), all within GxP environments. We provide comprehensive support across the entire Validation Life Cycle, including development studies.
Quality Support
We provide a comprehensive range of services, which include the development and approval of validation documentation (such as IO/OQ/PQ protocols), conducting quality investigations (including OOS events, stability failures, and equipment excursions), and managing product complaints in accordance with regulatory standards (medical devices—21 CFR Part 820; finished pharmaceuticals—21 CFR Part 211). Additionally, we offer risk management and data integrity support, as well as technical documentation services covering the creation and revision of procedures, specifications, user requirements, design documents, trace matrices, and validation plans.