Search for tag: "informed consent"

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01:01:29 Respecting Persons – From Basic… Respecting Persons – From Basic Requirements to Embracing Participant- Centered Informed Consent	Respecting Persons – From Basic Requirements to Embracing Participant- Centered Informed Consent This presentation reviewed ethical principles, discussed regulatory requirements for informed consent, and offered strategies to develop high-quality, participant-centered informed consent documents… ethics irb human research informed consent consent participants participant study requirements participation document subjects decision elements context questions rule words requirement person signature waiver documents question From Lisa Ballance 1 plays 0
57:11 Central VA SOCRA Chapter: Decentralized Clinical… Central VA SOCRA Chapter: Decentralized Clinical Trials: The Pros and Cons	Central VA SOCRA Chapter: Decentralized Clinical Trials: The Pros and Cons This Central VA SOCRA Chapter Meeting was recorded September 15, 2021. Andrew Cohen, MPH, Director of Global Healthcare Partnerships at Science 37. Mr. Cohen discussed Decentralized Clinical Trials… investigator protocol dencentralized clinical trials informed consent research participant From VCU CCTRSOCRA 31 plays
01:08:11 Central VA SOCRA Chapter: GDP on the Informed… Central VA SOCRA Chapter: GDP on the Informed Consent Process - From Good to Great	Central VA SOCRA Chapter: GDP on the Informed Consent Process - From Good to Great This Central VA SOCRA Chapter Meeting was recorded Wednesday, July 21, 2021. Jeannie Farnsworth, MS, BS, CCRP, MRQA, Sr. Research Compliance Analyst at Banner Health, Phoenix, AZ. Ms. Farnsworth… informed consent good documentation practice gdp human research clinical trial clinical research quality research trial From VCU CCTRSOCRA 56 plays Data Classification CATEGORY I DATA
58:10 Central VA SOCRA Chapter: The Ethics of… Central VA SOCRA Chapter: The Ethics of Volunteers Paying to Participate in Clinical Trials	Central VA SOCRA Chapter: The Ethics of Volunteers Paying to Participate in Clinical Trials This Central VA SOCRA Chapter Meeting was recorded Wednesday, May 19, 2021. Annette Oeser, Clinical Coordinator, Division of Clinical Pharmacology, Vanderbilt University, MLAS, discussed and… participants funding pay disease plasma irb benefit risk criteria oversight treatment influence consent quality clinical research complinace compensation informed consent From VCU CCTRSOCRA 33 plays
46:18 Central VA SOCRA Chapter: Educating Prospective… Central VA SOCRA Chapter: Educating Prospective Subjects About Their Role As A Research Subject	Central VA SOCRA Chapter: Educating Prospective Subjects About Their Role As A Research Subject This Central VA SOCRA Chapter Meeting was recorded Wednesday, March 17, 2021. Laura Holtz Senior. Research Manager, Indiana University Center for Aging Research and Regentrify Institute, discussed… research subjects research participants informed consent From VCU CCTRSOCRA 42 plays