Effective regulatory information management (RIM) tools and processes are needed to ensure BioPharma and Medical device companies are efficiently and effectively conducting life-cycle management and developing new products while also remaining compliant with approved product registrations.
Regulatory Information Management is dedicated to strategies on interpreting the regulatory requirements for filing, best practices for managing information, and review of many new or changing regulatory requirements, including:
Standards related to submission of regulatory information
Key issues shaping the global regulatory environment
Associated implementation experiences and lessons learned
The tools necessary to effectively manage the information
Regulatory Information Management brings together attendees involved in: