Biotechnology, medical devices and pharmaceutical companies are subject to many complex regulations. Combined with the volume of data contained in common business applications and the critical role that data plays in a company’s success, such regulations could create the perfect storm for any migration project. The reality is that manual sampling approaches, while theoretically defensible to the FDA, deliver migration results to production systems with “acceptable error.”
“Valiance excels in professionalism, customer service and client satisfaction. I truly appreciate the sense of teamwork and partnership they brought to this project.” – Project Director & CTMS Migration Project Lead, Global Contract Research Organization
Valiance is the specialist you need to execute your migration projects correctly. With over 500 migrations for 80+ customers globally, we bring the most capable GxP migration software and methodology and are fluent with relevant business processes and regulations that govern your industry.
Migrations are a complex undertaking and traditional testing approaches often fall short of today’s business and compliance requirements. The ensuing risk can easily result in costly errors. The question is: How sound are your current testing and sampling approaches?