Regulatory Information Management 2014

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 2014 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

Who should Attend

Attendees involved in:

• eClinical
• Clinical Research & Development/Clinical Supplies
• Information Technology
• Global Project Managers
• Regulatory Information Management
• Regulatory Affairs/Operations
• Regulatory, Medical, and Technical Writers