Live Webinar
on
Research Process from Discovery to Drug Marketing
Date & Time: Tuesday, September 6, 2011
10:00 AM PDT | 01:00 PM EDT
Duration: 60 Minutes
Instructor: Gbolahan Fatuga
Location: Online
Price : $245.00
Register Now
(for one participant)
Instructor Profile:
Overview:
Gbolahan Fatuga CEO, Caligeo Clinical CRO
This webinar will provide a clinical and regulatory perspectives on requirements to take a new drug from research to market. W e will begin by reviewing the contents of an Investigational New Drug (IND) application, and then follow the process of an IND submission.
Areas Covered in the Session:
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High level overview of the FDA approval process for a new drug What is an IND? Identify the key contents of an IND What is an NDA? Identify the contents of an NDA The FDA IND and NDA review process Discovery stage Preclinical Testing IND Application Clinical Trials Phases I to IV NDA High-level description of medical device process
Click here to register for this webinar
Fatuga is a social-entrepreneur who is actively engaged in three primary roles/companies: (a) founder/president of Caligeo Clinical OneVision; (b) founder/CEO of Caligeo Clinical CRO; and (c) founder/Executive Director of Atlanta Premier SMO. His professional passion lies in promoting clinical trial opportunities in emerging markets (especially in Africa, the Caribbean, East Asia, and Latin America) and among under-represented population (in the USA). He recently completed his MBA degree from Emory University/Goizueta Business School with a focus on Entrepreneurial ship/Organizational Behavior & Management. ...more
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Who Will Benefit: l l l l l
CRAs CRCs Nurses
Clinical Trials Associates Regulatory Affairs
It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely benefit from this program. For more information, please contact the event coordinator. We look forward to seeing you at the webinar. Best regards, Event-coordinator GlobalCompliancePanel
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