Αποτελέσματα Αναζήτησης
15 Σεπ 2023 · Schedule of Events Template – Version 09/15/2023. Purpose. All protocols that require an OnCore calendar need to have a Schedule of Events (SOE) that is in the form of a table listing the study visits as a timeline, and the procedures and events associated with each visit.
The templates below have been shared by other groups, and are free to use and adapt for your researchstudies. Please ensure that you read and adapt them carefully for your own setting, and that you reference Global Health Trials and The Global Health Network when you use them.
13 Μαΐ 2019 · Download free clinical trial templates for your clinical research, available in SharePoint, Word, Excel, and Microsoft Project formats.
Serious Adverse Event Form (MS Word, 31K or screen-readable PDF, 769K) provides a template for a study form for collecting information about serious adverse events. The form includes major components of the Food and Drug Administration (FDA) Form 3500.
Study teams should review all available tools and what will be needed for compliant and complete documentation. CRRO templated tools are built upon a mix of institutional policies, federal regulations, ICH Good Clinical Practice, and current best practices.
20 Ιουν 2024 · NIAMS-funded investigators are encouraged to use the NIH/NIAMS tools and templates when developing their study documents. For further guidance or questions, reach out to the NIAMS Clinical Research Operations and Management Branch at NIAMSclinicaltrials@mail.nih.gov.
8 Νοε 2022 · Every clinical research study involves many intervention and observation activities that must be performed by an investigator for a clinical trial participant. Typically, this is described in the study protocol as a succession of activities with a permissible interval between each one.
