A research assistant
obtained written informed consent from participating parents / guardians and assent from the youths and then administered the questionnaires in the waiting room of the pediatric and adolescent clinic.
We obtained written informed consent by all participants after the procedures were fully explained and the study was approved by the local ethical committee.
Human discarded foreskin tissues were obtained from the Shanghai Children's Center upon the approval from the Ethical Review Board of the Institute of Health Sciences and after
obtaining the written informed consent from parents of the child participants.
All patient material for this study was collected after
obtaining written informed consent from participants and an ethical vote approving the study (Institutional Review Board: Ethics Committee of the Medical Faculty of Heidelberg University, Germany / Ethikkommission der Medizinischen Fakultät Heidelberg) according to ICGC guidelines (www.icgc.org).
If the parent / caregiver is happy to continue, the researcher will
obtain written informed consent from the parent to participate in the study.
Appropriate professional precautions must ensure that the client's well - being is not compromised and that no exploitation occurs, and should include consultation, supervision, documentation, or
obtaining written informed consent of the client;
Because of the difficulty of
obtaining written informed consent from each parent, the approved procedure for obtaining consent was such that head teachers consented on behalf of adolescents whose parents did not return the written information leaflets, indicating no objection to the study and their child's participation.
Not exact matches
«It is nevertheless a matter of concern that the collection of the data by Facebook may have involved practices that were not fully consistent with the principles of
obtaining informed consent and allowing participants to opt out,»
wrote Inder Verma, the Washington, D.C. - based journal's editor in chief.
All women gave
informed written consent to participate, and ethical approval was
obtained by the Medical Ethical Committee of the Maastricht University Medical Centre (registration no. 04 — 234/11 -4-009).
Informed written consent to participate in the HBDP was
obtained from all participants.
The regional ethics committees for medical research approved the study and
written informed consent was
obtained from the women.
The authors state that: «The study was approved by the Institutional Review Boards of our institutions... and
informed written consent was
obtained from the patient.»
Human CD4 + T cells were
obtained after
written informed consent and approval by the University of Pennsylvania's institutional review board.
The study protocol was approved by the Institutional Review Board of Columbia University, and
written informed consent was
obtained from each subject.
Written informed consent was
obtained from the legal guardians of all patients.
Written informed consent was
obtained from all adult participants and the parents of minors.
Institutional review board approval was
obtained at each clinical center and all participants provided
written informed consent.
Written informed consent was
obtained from the parents of participating children after receiving a full explanation of the study.
Written informed consent was
obtained for all patient samples.
Separate
written informed consent was
obtained for screening and enrollment.
Written informed consent was
obtained from all mothers.
Oocytes, cumulus cells and frozen embryos were collected from Stanford Fertility and Reproductive Medicine Center after approval by the Stanford Institutional Review Board (IRB); all samples were
obtained with
written informed consent from all participants involved in the study.
Two patients who fulfilled the inclusion criteria were enrolled in the study and
written informed consent was
obtained.
At the appropriate time, the trainee
obtains permission to
write the dissertation, and the Training Committee is
informed of
consent.
Written approval for all somatic derivations and subsequent iPSC generation performed in this study was obtained from the Stanford University Institutional Review Board (IRB protocol 10368) and the Stanford University Stem Cell Research Oversight Committee (SCRO protocol 40), and written informed consent was obtained from each individual parti
Written approval for all somatic derivations and subsequent iPSC generation performed in this study was
obtained from the Stanford University Institutional Review Board (IRB protocol 10368) and the Stanford University Stem Cell Research Oversight Committee (SCRO protocol 40), and
written informed consent was obtained from each individual parti
written informed consent was
obtained from each individual participant.
Written informed consent was
obtained for all patients.
Written informed consent was
obtained from all subjects, and the study was approved by the Department of Veterans Affairs Medical Center and the University of Minnesota Committee on Human Subjects.
Written informed consent was
obtained from all participants.
Written informed consent was
obtained from all subjects.
Informed written consent was
obtained from each participant.
Written informed consent was
obtained from participants who then underwent health screening including: medical, psychological and sleep history, semistructured clinical psychiatric interview, physical examination, complete blood cell count and comprehensive metabolic panel, urine toxicology, 12 - lead electrocardiogram, and polysomnographic sleep disorders screen.
All subjects followed the same testing protocol and
written informed consent was signed and
obtained from the subject.
We will always honor referral fees and we will always put the agreement in
writing after
obtaining a client's
informed consent.
When asked, The Florida Bar stated that there is not a specific form to use when
obtaining informed consent, but it must be in
writing.
Written informed consent was
obtained from the participants in connection with baseline measures.
Written informed consent was
obtained for each participating child, and the study was approved by the Australian Institute of Family Studies ethics committee.
Written informed consent is
obtained from every participant.
Written informed consents were
obtained from parents prior to the screening process (12MMHIS188 approved by MacKay Memorial Hospital Institutional Review Board).
Before participating,
written informed consent was
obtained from their parents or guardians.
Written informed consent was
obtained for both mothers and children.
Written informed consent was
obtained from all subjects, and the study protocol was approved by the Ethics Committee of Inje University Ilsan Paik Hospital.
If you are not the responsible party, we must
obtain written consent of the legal guardian or other authorized legal representative prior to rendering services in the event the client is a minor child, an adult who is legally incompetent, or an adult incapable of giving
informed consent.
If
written informed consent is not
obtained, provide a sentence in the paper clearly explaining why not and what kind of
consent was
obtained.
Written informed consent was
obtained from all participants before joining the study.
Written informed consent was
obtained from parents before screening as well as during on - site visits and magnetic resonance scans.
After the study had been fully explained,
written informed consent was
obtained.
Written,
informed consent / assent was
obtained from parents and youths.
Written informed consents were
obtained from all parents or main caregivers of the students.
Written informed consent was
obtained after the interview procedures were fully explained.
Written informed consent was
obtained from parents.