FDA FDA 1501 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans Should Facilities exporting supplements to the U.S. must file prior notice? 1.31K viewsFDA 0 Votes 1 Ans What is a Full-time Equivalent Employee? 1.42K viewsFDA 0 Votes 1 Ans How Does Business Size Affect Preventive Controls Requirements? 1.19K viewsFDA 0 Votes 1 Ans What are the recently released numerous regulatory guidances to help the food and beverage industry comply with labeling rules? 1.28K viewsFDA 0 Votes 1 Ans How Do I Send an eCTD Submission? 1.10K viewsFDA 0 Votes 1 Ans Why does FDA requires manufacturers of certain RED products to have an accession number for their product prior to marketing it in the United States? 1.49K viewsFDA 0 Votes 1 Ans How Do I Get an Accession Number for my Laser Product? 1.16K viewsFDA 0 Votes 1 Ans Component or Accessory? What is the Difference in Medical Device? 1.11K viewsFDA 0 Votes 1 Ans What are the FDA’s New Accessory Classification Process on Medical Device? 1.41K viewsFDA 0 Votes 1 Ans Why did the the U.S. Food and Drug Administration (FDA) removed all drug establishments that did not renew their FDA registrations for 2018 from its active registration database? 1.44K viewsFDA 0 Votes 1 Ans What is Annual FDA Drug Establishment Registration? 1.18K viewsFDA 0 Votes 1 Ans What is the New “Blanket No Change Certification” Requirements for Drug Product Listings? 1.05K viewsFDA 0 Votes 1 Ans What are the responsibilities of an Official FDA Correspondent? 1.29K viewsFDA 0 Votes 1 Ans When Do I Need To Comply? 1.21K viewsFDA 0 Votes 1 Ans What are the new and updated information related to UDI and Global Unique Device Identification Database (GUDID) regulations? 1.36K viewsFDA 0 Votes 1 Ans Where GUDID Coordinators Able to Correct Errors After the DI Record Grace Period? 1.21K viewsFDA 0 Votes 1 Ans Why is FDA to make Premarket Numbers Public? 1.35K viewsFDA 0 Votes 1 Ans What are the FDA GUDID and UDI Requirements? 1.42K viewsFDA 0 Votes 1 Ans Why did the U.S. Food and Drug Administration (FDA) extended the deadline for the mandatory use of electronic common technical document (eCTD) format for type III Drug Master File (DMF) submissions by one year? 1.38K viewsFDA 0 Votes 1 Ans Does FDA Consider All Caffeine Supplements Adulterated? 1.03K viewsFDA « Previous 1 2 … 52 53 54 55 56 … 75 76 Next » Question and answer is powered by anspress.net