![Pharmaceutical sciences / FDA Special Protocol Assessment / Prescription Drug User Fee Act / New Drug Application / FDA Fast Track Development Program / Center for Biologics Evaluation and Research / Meeting / Investigational New Drug / Validation / Food and Drug Administration / Medicine / Health Pharmaceutical sciences / FDA Special Protocol Assessment / Prescription Drug User Fee Act / New Drug Application / FDA Fast Track Development Program / Center for Biologics Evaluation and Research / Meeting / Investigational New Drug / Validation / Food and Drug Administration / Medicine / Health](https://www.pdfsearch.io/img/bdb9613729a860a9a182c039635cf9ab.jpg) Pharmaceutical sciences FDA Special Protocol Assessment Prescription Drug User Fee Act New Drug Application FDA Fast Track Development Program Center for Biologics Evaluation and Research Meeting Investigational New Drug Validation Food and Drug Administration Medicine Health | | SOPP[removed]: Scheduling and Conduct of Regulatory Review Meetings with Sponsors and Applicants Version #5 Effective Date: October 15, 2012 I. PurposeAdd to Reading ListSource URL: www.fda.govDownload Document from Source Website File Size: 209,54 KBShare Document on Facebook
|