Science Researcher Update: Spotlight on Meetings, Conferences, and Events

What is the FDA position on the Responsibilities of the Principle Investigator while Conducting Premarket Clinical Research?

Posted on Jul 20, 2014 5:11:00 PM

 

Conference - Online

With the increasing surveillance / auditing by the investigative wing of the FDA / OHRP it behooves Physician and dentist Investigators to become familiar and knowledgeable regarding their responsibilities.To ‘think’ you know the rules of Clinical Research is not enough these days. When the PI signs the FDA form 1572 (for IND studies) or the "Statement of the Investigator (for IDE studies), she / he is signing a legally binding document committing themselves to follow all of the appropriate regulations.

Speaker: Charles H Pierce

Organization: Global Compliance Trainings

For more information, please visit: http://www.globalcompliancetrainings.com/index.php?route=product/product&product_id=29&list=Charles%20H%20Pierce

May 25, 2014 - May 25, 2014 (10:00 AM - 01:00 PM)

201, N Squirrel road, Suite 1007, Auburn Hills, Michigan United States - 48326

Contact: John Gordan (webinar@globalcompliancetrainings.com)

Phone: 2482120588

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Tags: 2014, Michigan, United States, Webinar, May, Quality Control, Clinical Research, Life Sciences, Conference, MI

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