Ethics Committee Sample Clauses
An Ethics Committee clause establishes a designated group or body responsible for overseeing ethical standards and conduct within an organization or in relation to a specific agreement. This committee typically reviews potential conflicts of interest, investigates ethical complaints, and provides guidance on ethical dilemmas that may arise during the course of business or project execution. By centralizing ethical oversight, the clause ensures consistent application of ethical principles and provides a clear process for addressing ethical issues, thereby promoting integrity and accountability.
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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. 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. 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. 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. 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 (▇▇▇▇ ▇▇▇ „EK“). Zdravotnické zařízení a zkoušející ▇▇▇▇ ▇▇▇▇▇ 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 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 systematické testování prováděné na subjektech hodnocení za účelem:
a) zjistit či ověřit klinické, farmakologické nebo jiné farmakodynamické účinky,
b) stanovit nežádoucí účinky,
c) studovat absorpci, distribuci, metabolismus nebo vylučování jednoho nebo několika hodnocených léčiv s cílem ověřit bezpečnost nebo účinnost tohoto hodnoceného léčiva.
Ethics Committee. The Collaboration will adhere to all relevant national and international rules and regulations regarding the environment, during construction, operation and decommissioning of the infrastructure. The RBB will install an Ethics Committee (EC) to actively review and monitor the compliance with these rules and any other ethical issues related to the construction, operation and decommissioning of the KM3NeT-phase1 Research Infrastructure. The Ethics Committee reports to the RRB and the IB.