DIAアカウントをお持ちの場合、サインインしてください。

サインイン

ユーザーIDをお忘れですか? or パスワードをお忘れですか?

Virtual Event

2020年5月18日 (月) 午前 10:00 - 2020年5月20日 (水) 午後 3:15

(US Eastern Standard Time)

Fort Washington, PA 19034

Advertising and Promotion Regulatory Affairs Conference

Session 4: Adding Value to Ad Promo Review, Tips and Best Practices: Panel Discussion

Session Chair(s)

Victoria  Tamarkin, MS

Victoria Tamarkin, MS

Founding Partner & President, Global Regulatory Affairs, Promotional Compliance

Victoria Tamarkin Consulting LLC, United States

Join a mock Medical/Legal/Regulatory (MLR) panel as they walk participants through their strategies for Ad Promo review. Panelists will explore case studies and discuss best practices for reviewing materials for different audiences and settings such as in social media and in convention booths at scientific congresses. Participants will learn how the panel views complex topics such as evaluating and applying the appropriate evidentiary standards that guide the review of different types of materials. Lastly, the panel will share best practices for effectively managing conflicting points of view and in this way furthering the contribution of each review discipline as part of a well-functioning promotional review committee.

Learning Objective :
  • Understand the types of medical, legal and regulatory considerations that apply to different types of materials and audiences including FDA Guidance, where applicable
  • Gain confidence in knowing the types of questions that a reviewer will want to ask
  • Find themselves better equipped on how to manage tension/conflict in Promotional Review Committees (PRCs)
  • Learn practical tips to collaborate and add value within cross-functional MLR and Commercial teams

Speaker(s)

Danielle Asuncion Carreon, MPH

Speaker

Danielle Asuncion Carreon, MPH

Bristol-Myers Squibb, United States

Director, Regulatory Affairs

William  Aprea, JD

Speaker

William Aprea, JD

(former) Bristol-Myers Squibb, United States

Executive Director, Senior Franchise and Compliance Counsel

Richard  Gersh, MD

Speaker

Richard Gersh, MD

Merck & Co., Inc., United States

Executive Director, Global Medical Affairs

最新情報や機会を逃さないで

DIAのメールを購読すれば、常に最新の業界情報やイベント情報を得ることができます。