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?

Boston Convention and Exhibition Center

2013年6月23日 (日) 午前 8:30 - 2013年6月27日 (木) 午後 12:45

415 Summer Street, , Boston, MA 02210 , USA

DIA 2013 49th Annual Meeting: Advancing Therapeutic Innovation and Regulatory Science

Electronic Submissions in PDUFA V

Session Chair(s)

Nancy D. Smith, PhD

Nancy D. Smith, PhD

Adjunct Professor

Temple University, FDA Alumni, United States

CDER will present an update and report on PDUFA performance goals and requirements related to electronic submissions. These include the requirement of electronic submissions and development of clinical and nonclinical terminology standards.

Learning Objective : Discuss how the PDUFA V performance goals affect electronic submissions requirements; Explain the steps CDER is taking to implement these goals, and the timeline in which they will occur.

Speaker(s)

Mary Ann  Slack

eData Standards: Where Are We

Mary Ann Slack

FDA, United States

Director, Office of Strategic Programs, CDER

Mark A. Gray

PDUFA V Electronic Submission Requirements: eCTD Update

Mark A. Gray

FDA, United States

Senior Project Manager, DSB, CBER

Steve  Wilson, PhD

CDER Perspective

Steve Wilson, PhD

FDA, United States

Senior Staff Fellow, OB, OTS, CDER

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。