Regulatory Information Management 2014

IMC Event
Date: Tuesday, 25 February 2014 - Wednesday, 26 February 2014

Venue: North Bethesda, MD, USA

With an increased focus on getting innovative therapies to market, ensuring patient safety and regulatory compliance with approved application information, organizations are challenged to operate with a global perspective. The ability to access and use information in the data-rich world of the BioPharma and Medical device industries is critical to success. Effective regulatory information management (RIM) processes and tools are needed to ensure organizations are effectively and efficiently developing new products and conducting life-cycle management while also remaining compliant with approved product registrations. This two-day annual conference will share strategies on interpreting the regulatory requirements for filing, best practices for managing information, and review of many new or changing regulatory requirements.


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