We provide end-to-end solutions with expertise in project planning, CQV master planning, requirement specifications, risk assessments, commissioning, decommissioning, FATs, SATs, installation qualifications, operational qualifications, performance qualifications, summary reports, traceability matrixes, calibration, temperature and humidity mapping services, and more. PSC Biotech® engineers readily facilitate greenfield facility startup services and facility remediation services with integrated commissioning and qualification (ICQ), Good automated manufacturing practice (GAMP), Continued process verification (CPV), Pre-Operational Verifications, Validation and Verification (V&V), Processed Analytical Technology (PAT) capabilities. PSC Biotech® has commissioning engineers to assist you in projects large or small. PSC Biotech® has the experts you need for services ranging from creating a validation protocol format, a validation master plan (VMP), training, technical audits, and due diligence to software validation, paperless validation, and more. The PSC Biotech® CQV team consists of seasoned experts in validating facilities, utilities, equipment, computer systems, processes, cleaning, test methods, and more.
PSC Biotech® is one of the largest providers of Commissioning, Qualification, and Validation services in the life science industry.
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