Templates for Clinical or Epidemiological Research
What Are Research Templates?
Research templates are pre-established forms designed to guide you in conducting your research and preparing submission files. INSPECT-LB is suggesting the following documents to help you throughout the process: study proposal, written consent form, ethical approval form, and conflict of interest (COI) declaration.
For INSPECT-LB Members
These templates are required when asking for funds or seeking ethics approval from INSPECT-LB.
Contributors
Authors: Danielle Badro; Hala Sacre; Danielle Saadeh; Jihan Safwan; Samah Tawil; Zeina Akiki; Nathalie Lahoud
Developer: George Choueiry
Supervisor: Pascale Salameh
References
1. FDA Office of the Commissioner. Regulatory Information. Food & Drug Administration. March 7, 2024. https://www.fda.gov/regulatory-information
2. Office for Human Research Protections (OHRP). Regulations, Policy & Guidance. U.S. Department of Health and Human Services. February 16, 2016. https://www.hhs.gov/ohrp/regulations-and-policy/index.html
3. NIH Office of Intramural Research. Office of Human Subjects Research Protections. U.S. Department of Health and Human Services. https://irbo.nih.gov/confluence/
4. University of California San Francisco. Verbal, Electronic or Implied Consent (Waiver of Signed Consent). Human Research Protection Program (HRPP). September 27, 2023. https://irb.ucsf.edu/verbal-electronic-or-implied-consent-waiver-signed-consent
5. Office for Civil Rights (OCR). Health Information Privacy. U.S. Department of Health and Human Services. June 9, 2021. https://www.hhs.gov/hipaa/index.html