Webinar On The FDA Drug Approval Process
Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1221 |
Category Food, Drugs & Biologics
Deadline: April 30, 2104 | Date: April 30, 2104
Venue/Country: Mississauga, ON, Canada, Canada
Updated: 2014-04-26 20:04:04 (GMT+9)
Call For Papers - CFPThis web seminar provides an overview of the entire FDA Drug Approval Process. This seminar will cover FDA requirements from discovery.We will begin by developing a molecule, testing it, going through the IND process, clinical testing and finally the NDA process. We will also discuss IND/NDA submission preparation, in-vitro studies, nonclinical studies and human clinical trials. Also discussed will be the underlying scientific and regulatory principles involved in the entire Drug Development Process. This web seminar will also provide a foundation of knowledge for those who require an understanding of the entire FDA Drug Approval Process.Areas Covered in the Session :Understand the FDA drug research requirementsLearn about IND processLearn about Clinical testing requirementsLearn about NDA processLearn about in-vitro and nonclinical testingWho Will Benefit:Regulatory Affairs PersonnelQuality PersonnelClinical PersonnelResearch PersonnelManufacturing PersonnelDrug Discovery PersonnelLegal PersonnelPersonnel who require a general understanding of the FDA Drug Approval ProcessContact us:Compliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V6, Canada Customer Support :416-915-4458 Email : email@example.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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