PPT-ICF Process IRB Webinar 11/13/2014

Objectives To recognize how to conduct an adequate informed consent process in adults and children To learn how to manage the process in special situations To identify things to avoid when documenting the process. Having a standardized and scientifically constructed test delivered by credentialing organization is a globally recognized way to elp ensure the fairness and strength of the ICF C redential The exam is intended as an assessment of knowledge Actual a Facilitator: Susan Carlisle. March 24, 2014. New ICF Credentialing Requirements . www.coachfederation.org. WHY THE CHANGE?. The ICF is taking a proactive stance in implementing Credentialing program improvements.. General Procedures for Ceding IRBMED Oversight. Procedures Specific to Chesapeake IRB. Medical School. Institutional Review Board (IRBMED). Introductions . Representatives. . Chesapeake. . IRBMED. Medical School. April 22, 2015. Pete Van Runkle. State Budget Agreement. Executive Budget (DODD) was mixture of good things and challenging things. Widespread concern about DODD proposal and actions of providers and families. Agenda. GRU IRB Development and Changes. WIRB-Copernicus Group. Process for transfer of Chesapeake IRB protocols. Process for the new WIRB submissions. GRU IRB Development and Changes. WIRB and IRBNet. May 19, 2017. Topics. Drivers for Centralized IRB Review. Regulatory changes . Trial Innovation Network. How JHM IRB will address the Single IRB requirements . Key Decisions. When JHM is serving as the IRB of Record. Mission Statement. The International Crystal Federation (ICF) is an organization of the world’s leading crystal manufacturers, distributors and support organizations.. The mission of the ICF is to serve as an advocate for the crystal industry in the areas of governmental relations, trade relations and consumer education.. Hila Berger, Director Research Integrity and Compliance. Mylka Biascochea, Compliance Coordinator IRB/IACUC. 1. Objectives . What is the Institutional Review Board (IRB) responsible for? And why?. What is Human subjects research?. Amy Krenzer, CIP, IRB Coordinator. Hila Berger, MPH, CIP, Research compliance Officer. 1. Objectives . What is the Institutional Review Board (IRB) responsible for? And why?. What is Human subjects research?. Question: What is "CIHI" and how does it relate to the North American Collaborating Centre (NACC) for the Family of International Classifications? Answer: The NACC has worked collaboratively with Towards aCommon LanguageFunctioning Disability and HealthThe International Classificationof Functioning Disability and HealthIntroduction 2ICF and the WHO Family of Classifications 3The need for ICF 4 Institutional Review Board. What is an IRB?. What is its job?. What are its guiding Principles?. Belmont Report (i.e., Respect for Persons, Beneficence, Justice). Code of Federal Regulations, Title 45 – Public Welfare, Part 46 Protection of Human Participants (aka . sIRB. ) Adoption & Evaluation Webinar. Once you’ve logged into WebEx, please select one of the following audio options:. Call Using Computer. I Will Call In. DO NOT SELECT the “Call Me” option.. Mary Eckart, BS, CIP, VA Central IRB Manager . Mikaela Myers, MA , VA Central IRB Manager. Jessica Kroll, MA, CIP, VA Central IRB Administrator . Webinar Housekeeping. Recording. - This session is recorded, and the associated handouts will be available on ORPP&E’s Education and Training website within a week after the webinar..