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Regulating a Social World

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Continuing Education credit or Certificate Program units are not available for the archived offering.

This archived webinar will be available for purchase through July 17, 2014.

With the explosion of social media and its growing importance, it’s critical for those in the pharmaceutical industry to understand how to leverage social networks compliantly to see positive results and minimize risk. If and when the FDA guidance on social media is final, questions will remain. This webinar will help the audience incorporate the latest social media technologies into acceptable and successful communications and marketing plans. Focus will be given to regulatory requirement, types of communications, responsiveness, and dealing with AEs.

This webinar is an initiative from the Regulatory Affairs Community.

Featured Topics 

  • Explosion of Social Media Usage & Its Growing Import
  • Status of FDA Guidance on Social Media
  • Relevant FDA Enforcement Activities
  • Key Regulatory Requirements
  • Four Types of Communications
  • Challenges for Social Media

Who Should Attend 

  • Advertising & Promotion
  • Regulatory Affairs
  • Medical Writing
  • Medical Communications
  • CMC

Learning Objectives 

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

  • Discuss how to leverage social networks compliantly
  • Identify the latest social media technologies that are acceptable and successful communications and marketing plans
  • Describe regulatory requirements, types of communications, responsiveness, and dealing with AEs.

Contact Information 

Printable Registration Form

Registration Questions
Elizabeth Espich, Customer Service Associate
Phone +
Fax +1.215.442.6199

Questions about this Archived Webinar
Carolyn Callahan
DIA North America
Phone +1.215.442.6194
Fax +1.215.442.6199

Technical Requirements 

Click here for minimum system requirements.


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Day 1 Thursday, Jul 18, 2013

  • 1:00PM - 11:59PM

    Regulating a Social World


    • Regulating a Social World
      Dale A. Cooke
      Vice President/Group Director, Regulatory Review
      United States

Registration Fees 

Other Fees

Government (Full Time) Individual
Charitable Nonprofit/Academia Individual
Group Site
Group Plus


Member Individual


NonMember Individual
Group Discounts

  • Group site registration is a license for ONE internet login allowing multiple viewers from one location.
  • Group Plus is a license for up to FIVE internet logins allowing one or more viewers at each login location.

No refunds will be provided in the event of a participant’s cancellation since all costs for this webinar have been prepaid by DIA. DIA reserves the right to modify or cancel programs and/or substitute presenters or panelists. DIA is not responsible for failure to deliver programs due to circumstances beyond its control.

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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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.

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