At CPDC, we are proud to offer specialized Quality and GMP advisory services tailored to the unique needs of the Canadian radiopharmaceutical industry.

While Good Manufacturing Practices (GMP) are a global standard to ensure the safety, purity, and efficacy of pharmaceutical products, radiopharmaceuticals present distinct and complex regulatory challenges. With over 15 years of experience in both clinical and commercial applications, CPDC has developed and implemented robust GMP quality systems that have consistently met the highest standards during regulatory inspections and client audits.

Our team brings deep expertise in navigating the intricacies of radiopharmaceutical production, offering flexible and scalable solutions that integrate seamlessly with your existing systems and teams. Whether you require support for initial GMP assessments, audit readiness, or ongoing quality assurance operations, CPDC delivers end-to-end guidance to help you achieve and maintain compliance across all stages of the manufacturing and control process.