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Regulatory Information Management (RIM)

Sep 21 2014 1:00PM - Sep 21 2014 4:30PM | Omni Shoreham Hotel 2500 Calvert Street NW, Washington, DC 20008 USA

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Overview 

Audience members will interact with tutorial leads to discuss the definition of “RIM,” data flows and integrations across RIM systems, current standards, important process considerations and roles and responsibilities across regulatory departments and systems.  The RIM Tutorial will provide attendees with an overview of the IT systems typically in use within the regulatory space. Attendees will also have a chance to discuss the future of RIM systems and standards. For more information please follow this link.

Who Should Attend 

Professionals in regulatory affairs, regulatory operations or other related functions who are working to define or re-define their Regulatory Information scope, tools or processes.  Anyone looking to expand their knowledge regarding IT systems used in the regulatory space, issues and considerations when thinking about installing, upgrading, or replacing regulatory systems, or changing roles and responsibilities or processes.

Learning Objectives 

At the conclusion of this tutorial, participants should be able to:

  • Define the full scope of "Regulatory Information Management"
  • Describe systems typically in use in the RIM space
  • Explain high level RIM processes, data flow, standards
  • Identify typical roles and responsibilities across regulatory and other functional area departments
  • Discuss the future of RIM with respect to systems, process and standards

Contact Information 

Registration Questions
Customer Service Department
Toll Free: 1.888.257.6457
Phone: +1.215.442.6100
Fax: +1.215.442.6199
CustomerService@diahome.org

Agenda Details
Carrie Dunn, Content Lead
Phone +1.215.442.6181
Fax +1.215.442.6199
Carrie.Dunn@diahome.org

Event Logistics
Ellen Diegel, Event Planner
Phone +1.215.293.5810
Fax +1.215.442.6199
Ellen.Diegel@diahome.org

Instructor(s) 

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Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

Participants with Disabilities:
Reasonable accommodations will be made available to persons with disabilities who attend an educational activity. Contact the DIA office in writing at least 15 days prior to event to indicate your needs.

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