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fbi-s-infragard -> fdr-s-impact
fda-experience-w -> fda-overview-pro
FDA Overview of FSMA’s Proposed Produce Safety Rule and Chamberlain Farms Environmental Assessment
FDA Experience with End of Phase IIa Meetings: An Attempt to Improve Drug Development Decisions
FDA Fühlt Nutzen Von Cannabidiol An
FDA FACTS: E-COLI OUTBREAK IN PRODUCTS CONTAINING SPINACH
美国 《FDA 食品安全现代化法案 》 概述 FDA Food Safety Modernization Act
美国 《FDA 食品安全现代化法案 》 FDA Food Safety Modernization Act 第一二部分解读
FDA Field Survey of Powdered Formula Manufacturing
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
FDA Final Rule & Revised CTEP Guidelines for Expedited Reporting of Adverse Events
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
FDA Final Rule & Revised NCI Guidelines for Expedited Reporting of Adverse Events
FDA First Approved Human Clinical Trials of CRISPR Gene Editing For The Treatment of AIDS
FDA Food Defense Tools and Resources
fda food facility registration
FDA Food Facility Registration and FDA Certificates Services at FDAhelp
FDA Food Registration and FDA Certificate Services at FDAhelp
FDA Food Safety and Security Overview
FDA Food Safety Modernization Act
FDA Food Safety Modernization Act: A Primer by FDA
FDA Food Safety Modernization Act Michael Rogers, M.S. Director, Latin America Office Food and Drug Administration
FDA: Food Safety
FDA Food Safety Reform: Context and Goals
FDA Foods Program Update
FDA Foods Program Update
FDA Foreign Priorities, Inspections and Compliance
FDA Foreign Priorities, Inspections and Compliance
FDA Foreign Priorities, Inspections and Compliance
FDA Form 1572: What It Means Who It Includes
FDA Form 483 Frequently Asked Questions
FDA form 483 observations and warning letters - what is the difference
美国食品和药品管理局 (FDA) 的 《 食品安全现代化 法案 》( FSMA ) 下拟议的预防控制法规 – 关键要点
FDA Globalization Act of 2009 Summary & Status
FDA Gluten-Free Labeling Public Meeting
FDA Grants Priority Review for Sacituzumab Govitecan for the Treatment of Metastatic Triple-negative Breast Cancer
FDA Grants Priority Review for Sacituzumab Govitecan for the Treatment of Metastatic Triple-negative Breast Cancer
FDA Guidance for Industry: Assessment of Abuse Potential of Drugs: Overview, Issues and Framework for a Decision Tree
Presentation to BPAC Dec. 15, 2010 Robert Duncan, Ph.D.
Chapter Legislative Representatives Government Affairs Update
FDA Guidelines for Advertising Copywriters
FDA Health Canada World Health Organization
FDA Health Claims Regulations
FDA Hearing : Cardiovascular Safety of ADHD Medications in Children & Adolescents
FDA Hearing : Cardiovascular Safety of ADHD Medications in Children & Adolescents
FDA Hearing on Suicide and Antidepressants
FDA Hearing on UV Tanning Devices
FDA Hearing on UV Tanning Devices
FDA Hearings on the BPCI Act
FDA Hepatitis C Hearing Oct 19, 2006
FDA: History and Organization
FDA: History and Organization
FDA Hot Topics
FDA Human Factors of Medical Devices
FDA hydrolysis activity test
FDA hydrolysis activity test
FDA – IDSA - ISAP Workshop April 15, 2004
FDA – IDSA - ISAP Workshop April 15, 2004
FDA Import Detained | Food Safety Laboratory | United States
FDA Import Detained | Food Safety Laboratory | United States
FDA Import Detained | Food Safety Laboratory | United States
FDA Import Detained | Food Safety Laboratory | United States
FDA Import Detained | Food Safety Laboratory | United States
FDA Import Detained | Food Safety Laboratory | United States
FDA Import Detained | Food Safety Laboratory | United States
FDA Import Operations Embassy Training Seminar
FDA Import Operations Importation of Biologicals Workshop October 10, 2017 University of Michigan
FDA Import Operations Initiative-Opportunities & Challenges For Trade
FDA Import Operations Overview
FDA Import Operations Overview
FDA IND Review: Regulations and Challenges
FDA Indecision
FDA Indecision
FDA Industry Statistics Workshop Organizational Meeting January 25, 2010
FDA Industry Statistics Workshop Organizational Meeting January 25, 2010
FDA Industry Workshop Statistics in the FDA & Industry The Future
FDA Initiative:
FDA Inspection Policy and Best GMP Practices
FDA Inspection Preparation and Management
FDA Inspectional and Regulatory Enforcement Trends: Key Focus on Trends in Consent Decree
FDA Inspections
FDA Inspections
FDA Inspections of Investigator Sites
FDA International Food Investigator
FDA Interstate Travel Program Update
FDA Interstate Travel Program Update
FDA - INTRODUCTION TO DRUG REGULATION
FDA - INTRODUCTION TO DRUG REGULATION
FDA - INTRODUCTION TO DRUG REGULATION
FDA - INTRODUCTION TO DRUG REGULATION
FDA Investigates the Use of Oxytocin in Ghana
FDA IRB & Informed Consent Regulations 2009 VA IRB Chair Meeting October 7-8, 2009
FDA Issues Proposal to Amend the Medical Device Quality System Regulation
FDA job description
FDA Labeling Overview FDA Seminar Denmark, April 23-24, 2013
FDA LABELING
FDA – Latin America Regional Office US-FDA-LAO@fda.hhs
FDA Lawyer Capote – Top Rated FDA Attorney in Florida
FDA Lead Reviewer Summary W.L. GORE & Associates EXCLUDER Bifurcated Endoprosthesis A. Doyle Gantt and Dorothy B. A
FDA Legal & Regulatory Considerations for Biomedical Startups
FDA Manufacturing Subcommittee
FDA-Mandated Alternative to Bisphenol-A
FDA Marks Orphan Drug Act Milestone: 30 Year Recognition January 2013
FDA may authorise Pfizer’s Covid vax for kids under 5 in Feb
FDA Medical Device Enforcement and Quality System Update
FDA Medical Device Enforcement and Quality System Update
FDA Medical Device Quality System Introduction
FDA Medical Device Rules
FDA Medical Device Update
FDA Medical Devices: Auditing the GMPs
FDA Medical Devices: Auditing the GMPs
FDA Medical Imaging Drugs Advisory Committee
FDA & MOBILE/IT Applications
FDA Modernization Act of 1997 Workshop
FDA Nasal BA/BE Guidance Overview
FDA Needs to Counter Misleading Information
FDA-NIEHS Interagency Agreement
FDA/NIEHS Phototoxicology Research and Testing Laboratory & NTP Center for Phototoxicology
FDA NME & NCE
FDA/NSTA Web Seminar: Teach Science Concepts and Inquiry with Food
FDA ODAC AML in Older Individuals
FDA ODAC Meeting November 8, 2005
FDA Office of Enforcement and Import Operations Division of West Coast Imports
FDA Office of Women’s Health Funded Pregnancy and Lactation Related Studies: 2001 – 2008
FDA Office of Women’s Health Pregnancy Exposure Registry Website
FDA Oncologic Drugs Advisory Committee Pediatric Oncology Subcommittee
FDA or NOT? Not All LDTs are Alike
FDA Orphan Drug Designation 101
FDA & OSHA – New Reforms & Standards Affecting the Industry
FDA & OSHA – New Reforms & Standards Affecting the Industry
FDA Oversight of Cell Therapy Clinical Trials
fda oversight of tobacco products: the good the bad and the ugly
FDA Overview of Antibiotic Regulatory Activities
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