PSC was founded in 1996 with the vision of providing life science companies mission-critical professional services to ensure their healthcare products are manufactured to the highest standards and mee...
PSC was founded in 1996 with the vision of providing life science companies mission-critical professional services to ensure their healthcare products are manufactured to the highest standards and meet all regulatory requirements. Over the last nineteen years we have grown and diversified to become a one-stop service and solution provider that offers life science consulting, quality management software, contract pharmaceutical manufacturing, and strategic and investment advisory services to more than 350 clients in more than 23 countries worldwide. PSC's offices are strategically positioned around the globe to maximize access to the world's pharmaceuticals, medical device, and biotechnology markets. PSC has five unique divisions within the parent company – each representing one of our areas of expertise: PSC Software, PSC Asia, PSC Biotech, PSC Investments and BioTechnique. Together, these divisions enable us to meet the ever-changing needs of our clients with a commitment to excellence and superior quality. PSC Biotech Corporation, headquartered in Southern California, is a global, multidisciplinary Life Science consultancy. As an industry leader in validation, compliance, and calibration services, PSC Biotech provides professional services in engineering, compliance, commissioning & qualification, validation, information technology, calibration, regulatory affairs, technical management, and quality control to biotechnology, medical devices, pharmaceutical, and diagnostics industries worldwide. PSC Biotech has its own software development team that builds enterprise software applications for auditing and compliance including: Auditutopia™, ACE. ACE is an enterprise quality management system (EQMS) that is trusted among highly regulated industries and reduces risk while improving efficiency. Our ACE EQMS system delivers collaboration capabilities and 21 CFR Part 11 compliant electronic signatures and audit trails to simplify regulatory reporting.