DIA会员及用户请点击登录

登录

忘记用户 ID? or 忘记密码?

Not a Member?

创建账户并加入。

Virtual Event

2021 年 03 月 08 日 9:45 上午 - 2021 年 03 月 10 日 5:05 下午

(US Eastern Standard Time)

Horsham, PA 19044

Advertising and Promotion Regulatory Affairs Conference

Session 1: FDA Update - What’s New and What’s Worth Reiterating

Session Chair(s)

Wayne  Pines

Wayne Pines

President, Health Care

United States

Catherine  Gray, PHARMD

Catherine Gray, PHARMD

Director, Office of Prescription Drug Promotion, OMP, CDER

FDA, United States

This session will feature senior representatives from CDER and CBER who will provide updates on recent FDA advertising and promotion activities, including compliance actions, process considerations, and goals for 2021.

Learning Objective : At the conclusion of this session, participants should be able to:
  • Demonstrate a thorough understanding of recent compliance actions
  • Identify best practices to construct and submit a Response to Compliance Action submission
  • Identify roles of the different CBER branches in Office of Compliance and Biologics Quality Division of Case Management
  • Explain best practices for communicating with your FDA colleagues

Speaker(s)

Catherine  Gray, PHARMD

OPDP Updates - Looking Back, Looking Forward

Catherine Gray, PHARMD

FDA, United States

Director, Office of Prescription Drug Promotion, OMP, CDER

Lisa  Stockbridge, PHD

Speaker

Lisa Stockbridge, PHD

FDA, United States

Branch Chief, Advertising and Promotional Labeling Branch, OCBQ, CBER

Deborah  Wolf, JD

Speaker

Deborah Wolf, JD

FDA, United States

Regulatory Counsel, OPEQ , Regulatory Policy, CDRH

Jason  Cober, MPA

Response to OPDP Compliance Actions in eCTD

Jason Cober, MPA

ProPharma, United States

Director Regulatory Review, AI, Digital Transformation

获得信息并保持参与

不要错失任何机会——请加入我们的邮件列表,了解DIA的观点和事件。