Validation & Engineering

 

QS Pharma has a dedicated Validation and Engineering Department, which uses its vast validation, cleaning, calibration, and facilities experience to maintain the GMP area, equipment, and utilities in a validated state and within regulatory compliance. The Validation and Engineering department works closely with QS Pharma's Quality Assurance (QA) to ensure that all regulatory and quality requirements are met. Our goal is to provide the GMP services required to ensure that any product manufactured at QS Pharma meets all regulatory submission and/or clinical trial requirements including the documentation required.