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’s automated data migration testing makes 100% verification of content and data feasible. Our in-depth knowledge of technologies and relevant applications include CAPA, clinical data management, clinical trial management systems, complaint systems, controlled document management, CRM, ERP, PLM, regulatory document management, safety data management and training management.
Our solutions get at the heart of making regulatory compliance as comprehensive as possible for specific regulatory bodies, including the US FDA, European Medicines Agency, Japanese Ministry of Health & Welfare and Canadian Health Product and Food Branch (HPFB).
Valiance is the specialist you need to execute your migration projects correctly. With over 500 migrations for 100+ 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.