Ethics Committee. CHAPTERS may, but are not required to, create an “ethics committee” to advise the CHAPTER’s Board and membership regarding CAMFT’s Code of Ethics and procedures. However, no CHAPTER may establish its own code of ethics or make determinations regarding ethics-related cases. All such cases are subject to CAMFT’s Code of Ethics and procedures for handling such matters. Any ethics committee created by a CHAPTER is advisory only.
Ethics Committee. The Contractor must establish an ethics committee, operating under written policies and procedures, to provide input to decision-making, including end-of-life issues and advance directives.
Ethics Committee an independent body consisting of healthcare professionals and non-medical members whose obligation is to protect the rights, safety, and health of Study subjects and to provide assurance of such protection by, among other things, taking a position on Protocol, the suitability of Principal Investigators and adequacy of the Site (defined further below), and on the methods and documents to be used to inform Study subjects and obtain their Informed consent.
Ethics Committee. Before the Trial is initiated, Institution and Investigator will ensure that the Trial is approved by the EC. Institution and Investigator will further ensure that the Trial is subject to continuing oversight by the EC throughout its conduct.
Ethics Committee. Chapters may, but are not required to, create an “ethics committee” to advise the Chapter’s Board and membership regarding CAMFT’s Code of Ethics and procedures. However, no chapter may establish its own code of ethics or make determinations regarding ethics-related cases. All such cases are subject to CAMFT’s Code of Ethics and procedures for handling such matters. Any ethics committee created by Chapters is advisory only.
Ethics Committee. Hospital and/or Investigator shall submit an Ethics Committee Application and the Protocol for approval to Hospital Ethics Committee. The Ethics Committee's unconditional approval of the Protocol and patient consent form is a prerequisite of participation under and compensation by this Agreement.
Ethics Committee. Before the Trial is initiated, Sponsor or its designee will confirm that the Trial has received written approval by the responsible ethics committee (the “EC”). Institution and Investigator acknowledge and agree that the Trial is subject to continuing oversight by the EC throughout the conduct of the Trial. Changes or supplements to the Protocol may be made by Sponsor from time to 2.5 Etická komise. Před zahájením studie zajistí zadavatel nebo jeho zástupce, aby studie získala písemné povolení od odpovědné etické komise (xxxx xxx „EK“). Zdravotnické zařízení a zkoušející xxxx xxxxx na vědomí a souhlasí, že studie bude i nadále předmětem dohledu ze strany EK po celou dobu jejího provádění. Čas od času může zadavatel provádět úpravy či dodatky protokolu po písemném oznámení zdravotnickému zařízení time, upon written notice to Institution and Investigator. If required by Applicable Law, changes to the Protocol must be approved by the EC and the applicable regulatory authority. a zkoušejícímu. Pokud to budou vyžadovat příslušné právní předpisy, musí změny v protokolu schválit EK a příslušný regulační úřad.
Ethics Committee. Prior to beginning the Trial, Sponsor shall provide to the Site documentation verifying approval by the Eth- ics Committee of the Protocol and the infor- mation to be provided to potential subjects of the Trial to secure their informed consent. Site shall promptly notify Sponsor if the Ethics Committee takes, or gives notice of its intent to take, any action that could reasonably be ex- pected to affect the Trial.
Ethics Committee. 1. The Contractor's Member Advisory Committee shall establish, maintain, and provide support to an Ethics Committee and be accountable to the Governing Body on issues addressed by the Ethics Committee. The Ethics Committee shall be composed of administration and program staff and the community at large in the fields of primary health care, behavioral health, religion, law, and ethics to represent diversity of Participants.
2. Responsibilities of the Ethics Committee shall include the following:
a. Reviewing the ethical dimensions of medical, behavioral health, and non-clinical decisions on behalf of Participants and making non-binding recommendations;
b. Providing guidance to the Contractor's Governing Body and Member Advisory Committee on recurring behavioral health and medical-ethical issues;
c. Assisting in the development of procedures in documenting Advance Directives, living xxxxx, and general Participant health wishes as required by state and federal law; and
d. Providing needed staff training around ethical issues and concerns.
3. The Ethics Committee shall meet when directed to meet by the Contractor or the Department.
Ethics Committee. Before the Trial is initiated, Institution will ensure that both the Protocol and the ICF are approved by an Ethics Committee that complies with all applicable regulations. Institution and Principal Investigator will further ensure that the Trial is subject to continuing oversight by the applicable Ethics Committee throughout its conduct.
