WebbDownload the National PICF template featuring a tiered information framework: Part A presents general information, Part B contains study specific information with an informal … WebbUse this PICF for genetic research that is non-interventional OR genetic research that has an interventional component that does not involve research on a drug or device. Refer to …
Ethics Application - Clinical Trials and Research
Webb19 nov. 2024 · A template of a patient Informed Consent Form (ICF) for adult patients considering participation in a study being conducted under an IDE through the FDA’s EFS … WebbGuides, templates and forms Guidance for completing your application for HDEC review, templates, legislation, and regulations. Updated application and post approval forms These are not the final versions as they may change, but are indicative of the layout. how do you register with the fda
Participant Information Sheet and Consent Form Guidance …
WebbUNSW Sydney NSW 2052 Australia Telephone +61 2 93851000 Authorised by Deputy Vice-Chancellor (Research) UNSW CRICOS Provider Code: 00098G ABN: 57 195 873 179 WebbThis template is a guide only. ( If more than one Participant Information Sheet/Consent Form is required for your research project, please label the different forms clearly for the different participant groups. Please note that if there is a sub-study, a separate form is required. ( There are 23 numbered sections in this template. WebbThe PICF and all other project documentation must include a version number, and date in the footer on each page. This ensures the document is identifiable from other versions of the document, and allows the document to be tracked over time. The version and date will need to be updated each time an amendment is made. NHMRC PICF Templates how do you register with hpcsa