{"product_id":"fda-drug-approval-process-2026-07-15","title":"FDA Drug Approval Process","description":"\u003cp class=\"header-block-grey\"\u003eCourse Description\u003c\/p\u003e\u003cdiv\u003e \u003cp\u003eThis web seminar provides an overview of the drug development process and how the FDA approves new drugs. The Investigative New Drug (IND) contents and \u003cfont face=\"inherit\" size=\"-1\"\u003ethe New Drug Application (NDA) are described with reference to applicable FDA regulations and the phases of clinical trials required by the FDA.\u003c\/font\u003e \u003cfont color=\"inherit\" face=\"inherit\" size=\"-1\"\u003e\u003c\/font\u003e\u003c\/p\u003e \u003cp class=\"header-block-grey\"\u003eLearning Objectives\u003c\/p\u003e \u003cul type=\"disc\"\u003e \u003cli\u003eDescribe the FDA's role in drug development\u003c\/li\u003e \u003cli\u003eDescribe the basics of the clinical trial process\u003c\/li\u003e \u003cli\u003eDescribe the FDA review process for IND\/NDA submissions\u003cbr\u003e \u003c\/li\u003e \u003c\/ul\u003e \u003cp class=\"header-block-grey\"\u003eWho Should Attend\u003c\/p\u003e \u003cul type=\"disc\"\u003e \u003cli\u003eClinical Research Coordinators\u003c\/li\u003e \u003cli\u003eClinical Research Associates\u003c\/li\u003e \u003cli\u003eClinical Trial Managers\u003c\/li\u003e \u003cli\u003eClinical Project Managers\u003c\/li\u003e \u003cli\u003eRegulatory Affairs Personnel\u003c\/li\u003e \u003cli\u003eQuality Assurance Personnel\u003c\/li\u003e \u003cli\u003eManufacturing Personnel\u003c\/li\u003e \u003cli\u003eResearch Personnel\u003c\/li\u003e \u003cli\u003ePersonnel that have to understand the FDA new drug approval process\u003cbr\u003e \u003c\/li\u003e \u003c\/ul\u003e \u003cp class=\"header-block-grey\"\u003eInstructor\u003c\/p\u003e \u003cp\u003eLily Romero, P.A., C.C.R.C.\u003c\/p\u003e \u003cp\u003e\u003cspan class=\"purple-link\"\u003e\u003ca title=\"Click here for complete trainer biographies\" href=\"https:\/\/stage.barnettinternational.com\/instructor-biographies\"\u003eClick here for complete trainer biographies\u003c\/a\u003e\u003c\/span\u003e\u003c\/p\u003e \u003cp class=\"header-block-grey\"\u003eRegistration Fees\u003c\/p\u003e \u003cp\u003e$735*\u003c\/p\u003e \u003cp\u003e*Includes up to 20 participants per login at a single location. All participants (up to 20) are eligible for \"Certificates of Attendance,\" and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional logins for other locations, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing.\u003c\/p\u003e \u003cp class=\"header-block-grey\"\u003eAccreditation Information\u003c\/p\u003e \u003cp\u003eBarnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 2 hours (0.2 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-24-050-L99-P. Released: 9\/24. \u003c\/p\u003e \u003cp align=\"center\"\u003e\u003cspan class=\"bold\"\u003eHold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471. \u003c\/span\u003e\u003c\/p\u003e \u003c\/div\u003e","brand":"Barnett International","offers":[{"title":"Commercial","offer_id":52823803625837,"sku":"BI17305","price":735.0,"currency_code":"USD","in_stock":true}],"url":"https:\/\/www.barnettinternational.com\/products\/fda-drug-approval-process-2026-07-15","provider":"Barnett International ","version":"1.0","type":"link"}