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GPs and the British Medical Association have protested that explicit consent should be sought from each patient.
Site-specific approvals will be sought from each hospital.
Informed consent will be sought from each participant for the use of administrative data.
Judgements about the value of one's life should be sought from each individual, however this was not always possible to achieve.
Specific consent will be sought from each participating patient for access to their administrative health data and its use by the parties involved in the study.
Consent will be sought from each participant to record the interview, and will be stored electronically using the assigned identification number for each participant.
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A signed, written informed consent was sought from each participant only after a full explanation had been given, a patient information leaflet offered, and time allowed for consideration.
The following information was sought from each publication: the first author's name, year of publication, country of origin, ethnicity, cancer type, source of control (population- or hospital-based controls), genotyping method and number of cases and controls.
Informed consent was sought from each player.
Informed consent was sought from each participant.
Written Informed consent was sought from each respondent.
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