Regulatory Information Management 2014

  • 25-26 Feb 2014
  • Bethesda North Marriott Hotel & Conference Center, Rockville, MD, United States

Description

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

Regulatory Information Management 2014 brings together 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

Past Events

Important

Please, check "Regulatory Information Management" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma
Science: Life Sciences & Biology
Technology: Biotechnology, Information Technology (IT)

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