Faculty: Carolyn Troiano


  • Date: 11/3/2022 11:00 AM - 11/3/2022 12:30 PM
  • Location: Online Event

Tickets


Ticket Type
Qty
Live- Single
$250.00
0
For ONE Participant – Live session only
Live Corporate
$790.00
0
For Maximum of 10 participants – Live session only
Recording - Single
$390.00
0
Recording access for ONE participant (viewer) – Unlimited viewing access for 6 months
Recording - Corporate
$1400.00
0
Recording access (Multiple licenses) for up to 10 participants – Unlimited viewing access for 6 months

Total

$0.00

Description

This seminar will help you understand in detail the application of FDA’s guidance on the use of social media in presenting and promoting information about drug products and medical devices subject to FDA regulation. This is critical in order to develop the appropriate strategy, policies and procedures to ensure compliance.

This webinar will also benefit any consultants working in the tobacco or life science industries who are involved in computer system implementation, validation and compliance.

Areas Covered in the Session :

  • Pros and cons of using social media venues
  • Compliant use of Social Media in an FDA-regulated Environment
  • FDA draft guidance documents
  • Balancing benefit and risk information on social media
  • Managing character space limitations on social media
  • Managing misinformation posted by independent third-parties
  • Pending regulatory action by the US Congress

Who Should Attend:

  • Information Technology Managers and Analysts
  • Medical Affairs Managers and Analysts
  • Clinical Data Managers and Analysts
  • Marketing Managers and Analysts
  • Compliance Managers and Analysts
  • Regulatory Affairs Managers and Analysts
  • GMP Training Specialists
  • Business Stakeholders responsible for product presentation and promotional content
  • Consultants working in the life sciences industry who are involved in product presentation and promotional content