Our Principle : “Quality has Quality only if its Quality is Qualified”

The pharmaceutical and life sciences industry is among the most heavily regulated in the world. Today, these companies face unprecedented compliance challenges, and the close regulatory scrutiny to which they are subject is unlikely to abate anytime soon.

At no time have risk resilience and the need to effectively manage compliance been more important to the pharmaceutical and life sciences industry. Companies have to consider a wide range of emerging risks as they adapt their business to changing regulatory and marketdriven pressures, including globalization, the advancement of technology, and the changing expectations of stakeholders. New information systems, strategies and processes to manage compliance are rapidly evolving in response to these pressures.

Through a multidisciplinary team of industry, regulatory, and scientific specialists, Shadow helps organizations to prevent and resolve compliance problems and to develop efficient and effective strategies for the submission and approval of drugs, biologics, and devices. The company deploys only highly experienced who consistently delivers top-quality results for a diverse base of global clients-including pharmaceutical biologic, biotechnology, medical device, and dietary supplement companies and the law firms that serve them.