Summary:

Regulatory Affairs professionals in the pharmaceutical industry play the critical role of ensuring that a manufacturer is in compliance with regulatory bodies from pre-launch through the entire product life cycle.  Products that inadvertently slip into a state of non-compliance pose a great financial risk to companies.

An enterprise-wide approach to product registration tracking, integrated with change control and correspondence and commitment tracking provides a complete solution for RA professionals.  Using technology eases the administration burden, enabling RA professionals to work with greater efficiency and accuracy while reducing the costs and risks for the organization.