Ethics approval. The following arrangements have been made with regard to Ethic approvals: [insert from proposal template]
Ethics approval. The study has been approved both in France (IARC ethics committee, IEC) and Tanzania. The IEC requested that in the instance of an oesophageal cancer patient being diagnosed under age 18, they should NOT be recruited to the study. This is reflected in the eligibility criteria for cases. Accordingly, NO minors below the age of 18 years should be invited as controls. The Tanzania approval was granted under KCRI PI Prof. Kibiki and we are in the process of updating the Xx Xxxx Xxxxxxxxxx.
Ethics approval. Provider and Investigator will not initiate the Study or enroll any subject until after the competent authority and the relevant EC/IRB has approved the Protocol, Informed Consent Form (“ICF”), subject recruitment materials, as applicable, and Xxxxxxxx has received a written copy of such approval. Any alterations of, or amendments to the Protocol must be approved by Provider, Investigator, EC/IRB and Sponsor prior to such alteration or amendment becoming effective. Neither the Provider nor the Investigator shall implement any Protocol amendment until it is approved by the relevant authorities and the EC/IRB.
Ethics approval. 4.6.1 Spain (Aragon) Aragon Research Ethics Committees (CEICA). Decree 96/2013 This Decree is for the regulation of the Bioethics Committee of Aragon and Ethics Committees of Health and Social Centres.
Ethics approval. It is the investigator’s responsibility to ensure that this protocol is reviewed and approved by the appropriate local IEC or IRB. A non-local IEC or IRB may be used if a local one is not available. The IEC or IRB must also review and approve the site’s informed consent form (ICF) and any other written information provided to the subject prior to any enrolment of subjects, and any advertisement that will be used for subject recruitment. The investigator or his/her designee must forward to GW copies of the IEC or IRB approval and the approved informed consent materials, which must be received by GW prior to the start of the study. If, during the study, it is necessary to amend either the protocol or the informed consent form, the investigator will be responsible for ensuring the IEC or IRB reviews and approves these amended documents. IEC or IRB approval of the amended ICF must be obtained before new subjects consent to take part in the study using this version of the form. Copies of the IEC or IRB approval of the amended ICF and the approved amended ICF must be forwarded to GW as soon as available.
Ethics approval. In general, in order to respect at the highest possible level the care recipients enrolled in the Project, it is recommended that all sites look for an approval of the operational protocol by the local Ethical Committee. This seems particularly advisable to have a third party opinion on both the informed consent forms which will be submitted to all candidates, and on the general procedures of subsequent enrolment and follow-up. This is established even if no randomisation is employed and all enrolled subjects experience “non-usual integrated care”.
Ethics approval. The Institution acknowledges that the supply of the Original Materials to the Recipient is conditional upon the Institution obtaining approval for the use of the Materials in the Project from an appropriately constituted research ethics committee. The Institution will provide the Supplier with a copy of such approval prior to the Supplier making the Original Materials available to the Recipient. The Institution confirms that the potential benefits of the Project outweigh any potential risk to the Donor(s).
Ethics approval. If yes, will the organization provide one? If yes, will the student need to do anything? Confidentiality, Ethical, and Intellectual Property Issues Identify any privacy issues associated with field placement and products. Xxxxxxx who owns the research and how potential publication will be handled. Occupational Health and Safety Concerns Identify any health and safety concerns (e.x., students will be placed in environments with potential increased risk of injury or insecurity, potential contact with blood or other bodily fluids etc.) Funding from site: If yes, how much (Hourly? Stipend)? Other benefits, accommodations etc. The Field Supervisor agrees to: Provide the student with an appropriate work area (e.x., desk, computer, phone, fax, copier, analytics and other software etc.). Arrange a student orientation in the first week of the practicum. Accept the day-to-day responsibilities for the student, including assigning tasks and activities. Provide ongoing supervision and monitoring of student performance. Complete the interim and final evaluation forms, and discuss evaluations with the student before sending to Practicum Director. Inform the Practicum Director in a timely manner regarding concerns. Arrange for the student to present their practicum project work to an appropriate audience at the organization/agency. The Student agrees to: Be responsible for their own transport and living costs (unless otherwise specified). Meet with supervisor regularly. Meet professional standards of conduct including respecting confidentiality of information. Exhibit responsible behaviour regarding attendance and interest in agency activities. Enable the completion and submission of interim and final evaluation forms. Inform the Practicum Director in a timely manner regarding concerns. Evaluate the placement and practicum experience. Signatures of Practicum Supervisory Committee We hereby agree to the conditions outlined in this UBC MPH Learning Contract: Student Name (print) Student Signature Date Practicum Supervisor Name (print) Practicum Supervisor Signature Date If applicable: Practicum Supervisor 2 Name (print) Practicum Supervisor 2 Signature Date Please submit the completed form to the internal MPH course. To be filled by UBC MPH Program Office
Ethics approval. The Parties acknowledge that the Project may require approval by an institutional ethics and/or biosafety committees (or similar) of UNSW or the Participating Institutions. The relevant Party must use reasonable endeavours to promptly obtain that approval. Before such approvals are obtained, the Parties are not required to commence the Project.
