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?

Baltimore Marriott Waterfront

2024年2月05日 (月) 午前 7:00 - 2024年2月07日 (水) 午後 1:00

700 Aliceanna Street , Baltimore, MD 21202

Global Pharmacovigilance and Risk Management Strategies Conference

Register for 2 or more short courses and save $150 off your registration fee!

Hosted Session/Non-CE: Case Study Spotlight hosted by Caidya: Challenges and Opportunities with Safety Management and Reporting in Multinational Studies

Session Chair(s)

Representative Invited

Representative Invited

United States

As safety regulations and guidances are updated, Pharmacovigilance staff must remain aware of key differences to plan effectively, provide high quality reports, and ensure compliance with all timelines. This case study will provide example differences in national and regional requirements encountered in a multinational clinical trial involving safety data collection, serious adverse event (SAE) assessment, expedited and periodic reporting. Diligent regulatory intelligence and good team communication led to more robust study planning and Safety Management Plans. Periodic review of processes and plans continued to be needed as the study progressed

Featured Topics:

  • Ensuring diversity of clinical trials while remaining compliant with data protection requirements
  • Performing casuality and expectedness assessments of SAEs
  • Implementing ICH E2B (R3) regional elements
  • Registering and using regulatory reporting portals
  • Incorporating national and regional expectations into Development Safety Update Plans (DSURs)

Speaker(s)

Sharon  Moore, MD, MBA, MPH

Instructor

Sharon Moore, MD, MBA, MPH

Caidya, United States

Chief Medical Officer

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。