Clinical Compliance 2012 - Navigating the Japan Regulatory and Clinical Trial Environment; Conducting Clinical Studies in Japan
Date2012-03-09
Deadline2012-03-09
VenuePalo Alto, USA - United States
KeywordsFinancial Disclosure; Clinical Trials; FDA Guidance; marketing approval application; clinical investigator; co-investigator; sub-investigator
Topics/Call fo Papers
This Webinar will help you understand the current FDA requirements regarding financial disclosure in clinical trials. It will discuss differences from the older requirements, and tips to assure compliance all through from the start of clinical trials till the submission of data in a marketing approval application.
Why Should You Attend:
If your company or organization is sponsoring clinical trials for a drug, biologic medical device or a diagnostic kit; if you are a clinical investigator, co-investigator or sub-investigator participating in a clinical trial; if you are with an IRB overseeing clinical trials, or if you are senior management in a company sponsoring clinical trials, this webinar will help you understand the current FDA requirements regarding financial disclosure.
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Last modified: 2012-02-16 14:24:45