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。

Westin Arlington

2024 年 09 月 23 日 7:00 上午 - 2024 年 09 月 24 日 7:00 下午

801 North Glebe Road, , Arlington, VA 22203 , USA

Global Clinical Trial Disclosure and Data Transparency Conference

Learn about the latest requirements in clinical trial disclosure and data transparency, share best practices, and engage in in-depth discussions on hot topics.

Call for Abstracts Closes in

DAYS

HOURS

MINUTES

SECONDS

概览

September 23-24: Conference

Clinical trial information transparency is taking on new dimensions. Clinical trial sponsors and academia are facing a host of new registration requirements in the US, EU, and elsewhere. With evolving requirements comes new challenges, creating additional opportunities for knowledge-sharing and necessitating more interaction with peers. This conference will provide critical and timely information relating to global clinical trial disclosure and data transparency from those on the front lines.

While we develop our 2024 agenda, please take a moment to review the 2021 final agenda.

 

 

 

Need Approval in Order to Attend?

Download and fill out our Justification Letter to demand to supervisor why this is a must-attend event.

 

Participant Testimonials

Thanks for organizing such a nice conference on CTD and Trial Transparency. It was my first experience attending the DIA conference and I learnt new initiatives taken across industry.” – Ravi Jogai, Associate Director - Syneos Health (Seasoned Clinical Research Professional)

Featured

Want to learn more about Global Clinical Trial Disclosure and Data Transparency Conference? You've come to the right site!

Highlights & Features

谁应该参加?

  • Conference Designed For:

    • Academia
    • Biometrics
    • Clinical Operations / Development
    • Clinical Trial Disclosure
    • Clinical/Medical Research
    • Compliance/Legal
    • Data management
    • Data transparency/data sharing
    • External Health Authorities (comp and ethics committees)
    • Internal Regulatory / Regulatory Submissions/Regulatory Leads
    • Medical Writing, Medical Affairs, and Medical Communications
    • Patient Advocacy
    • Patient registries
    • Publications
    • Real-World Data
    • Transparency policies and compliance (Clinical Data)

项目委员会

  • Robert  Paarlberg, MS
    Robert Paarlberg, MS Principal
    Paarlberg & Associates LLC, United States
  • Kelly  Coulbourne, MS
    Kelly Coulbourne, MS Director, Clinical Trial Disclosure and Data Transparency
    Pfizer Inc, United States
  • Scott  Feiner
    Scott Feiner Senior Manager, Trial Disclosure
    AbbVie, United States
  • Francine  Lane, MBA
    Francine Lane, MBA Senior Director of Product Management
    Citeline, United States
  • Pritibha  Singh, MBA, MSc
    Pritibha Singh, MBA, MSc Senior Manager, Corporate Affairs Analytics & Insights
    Novartis AG, Switzerland
  • Merete  Joergensen, MBA, MSc
    Merete Joergensen, MBA, MSc Clinical Disclosure and Transparency Expert, Former EFPIA, CREG Clinical Trials
    Merete-J Consulting CVR: 34920818, Denmark

Digital Learning Catalog

DIA Learning: eLearning Soultions
Download

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。