FDA FDA 1501 Questions Ask question Search Order By: ActiveClear Filter 0 Votes 1 Ans When must clinical trial information for a “triggered trial” be submitted to meet the requirements for voluntary submissions under 42 CFR 11.60? 2.17K viewsFDA 0 Votes 1 Ans Why should I participate in medical research? 1.89K viewsFDA 0 Votes 1 Ans What should I expect if I join a research study? 1.78K viewsFDA 0 Votes 1 Ans What is informed consent? 1.91K viewsFDA 0 Votes 1 Ans Are there any risks involved in participating in a research study? 1.79K viewsFDA 0 Votes 1 Ans Will my privacy be protected if I take part in a clinical trial? 1.86K viewsFDA 0 Votes 1 Ans We make different devices at different establishments that are listed under the same device product code or submission number. Do we need to identify proprietary names on an establishment-by-establishment basis? 1.75K viewsFDA 0 Votes 1 Ans Now that a foreign establishment is required to provide the names of all known importers of its devices, must it continue to update this information in FURLS whenever it changes? 1.81K viewsFDA 0 Votes 1 Ans As an importer, I am now required to provide the manufacturer information for devices I will be importing. Must I update this information in FURLS as new firms are added or I decide to no longer distribute for a particular manufacturer? 1.68K viewsFDA 0 Votes 1 Ans I am a foreign exporter, contract manufacturer, or contract sterilizer and I am trying to list a non-exempt device and FURLS will not allow me to proceed. Why can I not list this device? 1.74K viewsFDA 0 Votes 1 Ans What are the different types of accounts in the FDA Unified Registration and Listing System (FURLS) that are used to access the Device Registration and Listing Module (DRLM)? 1.84K viewsFDA 0 Votes 1 Ans What registration information must I submit if my applicable clinical trial is required to be registered? 2.14K viewsFDA 0 Votes 1 Ans When must I submit the required clinical trial registration information? 1.91K viewsFDA 0 Votes 1 Ans How are examinations by telephone call or other electronic means considered in determining when an applicable clinical trial reaches its “primary completion date” or “study completion date” under the regulation? 1.80K viewsFDA 0 Votes 1 Ans At what point is a human subject considered to be “enrolled” in an applicable clinical trial? 1.90K viewsFDA 0 Votes 1 Ans What is the Primary Completion Date and/or Study Completion Date when an outcome is measured or assessed after a study participant has been examined or received an intervention for that outcome? 1.92K viewsFDA 0 Votes 1 Ans Am I required to submit results information for my applicable clinical trial (ACT)? 1.79K viewsFDA 0 Votes 1 Ans When is required clinical trial results information due? 1.96K viewsFDA 0 Votes 1 Ans Is a protocol and statistical analysis plan (SAP) required to be submitted? 1.66K viewsFDA 0 Votes 1 Ans What is the results information submission deadline for applicable clinical trials (ACTs) of drug, biological, or device products that are not approved, licensed, or cleared for any use and studied in conjunction with, or in comparison to, approved, licensed, or cleared products? 1.72K viewsFDA « Previous 1 2 … 63 64 65 66 67 … 75 76 Next » Question and answer is powered by anspress.net
