Spirometry data is pivotal to assessing primary or secondary outcomes in most respiratory trials, but implementation in a clinical trial varies by sponsor and service provider. A significant portion of spirometry data in clinical trials is of inadequate or questionable quality.
The webinar will:
- Describe and explain the main quality issues encountered in clinical trials
- Explore mitigation actions that can improve spirometry quality
- Discuss interpretation and impact of ATS/ERS guidelines on a clinical trial
- Help your team ensure spirometry is managed in a way that safeguards data integrity and transparency
- Provide considerations on device set-up and standardization
Who Should Attend:
- Clinical Operations
- Medical Directors
- Scientific Directors
- Outsourcing Professionals
- Global Trial Leaders
- Professionals involved with Respiratory Disease
Registration
Registration is complimentary.
A valid business Email address is required to attend.

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Webcast Information: |
Date: Nov 29th, 2016 |
Time: 12:00 pm ET
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Duration: 60 Minutes |
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Featured Speakers: |
Susan Blonshine
Principal Consultant
Pulmonary Function Testing and Quality Systems |
Lisa Pifalo, RRT
Senior Scientist,
Scientific & Medical Services
PAREXEL |
Bertrand Sohier MD
Senior Medical Director, Global Head, Respiratory/Cardiovascular
PAREXEL |
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