Webinars >>FDA Regulations
New Rules for Using Social Media in Marketing FDA Regulated Products
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Social media offers an excellent opportunity for a company to get the word out about its drugs, biologics, medical devices and diagnostic kits. However, FDA regulated products need to follow strict information control; any information distributed to consumers must be approved by FDA. This is hard with social media outlets where information can quickly get out of hand and lead to violation of FDA regulations, and possible penalties on the manufacturers.

The FDA recently held hearings addressing drug companies' use of social media and other online platforms to advertise. FDA also released a guidance document about manufacturers’ obligation regarding off-label information available about their products. Another guidance document about use of social media in marketing is expected soon. In addition, FDA issued several letters to manufacturers indicating the rules for using social media.

But there is still much confusion among FDA regulated companies how to use social media for marketing effectively and still be compliant with regulations. How can medical device, pharmaceutical and other FDA regulated industries use social media channels like Facebook, Twitter, YouTube and LinkedIn to get their message out in a way that is compliant with advertising and promotion regulations found in the Food Drug & Cosmetic Act? This presentation will present ways to use social media that are compliant with FDA regulations. Practical regulatory strategies will be suggested to ensure compliance and balanced social media activity.
Areas Covered in the Session:
  • How Direct-to-consumer-advertising (“DTCA”) guidance impacts the use of social media.
  • Common ways companies are currently using social media.
  • FDA advertising and promotion issues related to social media.
  • A structure for analysis of responsibility for promotion in social media.
  • Handling unsolicited requests for off-label information
  • Recent trends in FDA enforcement actions involving social media.
  • Recent discussions about social media in marketing of FDA-regulated products. 

Why should you attend:

The seminar will discuss the do’s and don’ts for using social media in marketing FDA-regulated products. Common issues, misconceptions, perceptions, and possible solutions will be discussed. In a social media rich environment, manufacturers cannot avoid information dissemination via social media, hence it is prudent to familiarize with the current processes and plan for developments expected in the near future.

Learning Objectives:

At the end of the seminar, the attendees will be familiar with the following:
  • Recent FDA guidance on controlling dissemination of information via social media
  • Common practices for using social media such as Facebook, YouTube, and Twitter
  • Meeting with FDA to discuss social media submissions
  • Trends in FDA review of social media information
  • Do’s and Don’ts for managing social media for marketing your product
Who will benefit: 

The following individuals or disciplines will benefit from attending this Webinar:
  • Clinical project managers
  • Clinical research associates
  • Clinical coordinators
  • Principle investigators
  • Compliance Managers
  • Regulatory Vice Presidents, Directors and Managers
  • Attorneys – In-house or Outside Counsel
  • Senior executives of pharmaceutical and device firms
Date: June 30, 2020
Time: 12 PM ET        
​Duration: 60 Minutes

Speaker:
Mukesh Kumar
PhD, RAC Brij Strategic Consultations

    For more info, fill the box below. We will contact you within 24 hrs.
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: info@fdamap.com