Skip to main content
editorial
. 2008 Apr;9(4):307–313. doi: 10.1038/embor.2008.41

Table 3.

Informed consent procedures to collect and store human biomaterials for research purposes applied in our hospital before the present study

Specialty (number of procedures) Reason for informed consent request Type of information on the storage and future use of samples and related data
Clinical pathology (n = 3) Diagnostic analysis Absent
Haematology (n = 9) Chemotherapy treatment Treatment with blood components Prenatal diagnosis of haemophilia A and B Participation in an international database on rare bleeding disorders Analysis of genetic heritage Absent Absent Absent Absent Absent
Surgery (n = 7) Removal of neoplastic tissues and organs Urethra reconstruction Generic Generic
Neurology (n = 4) Surgical biopsy Generic
Gynaecology (n = 4) Investigation on molecular markers Specific
Medical genetics (n = 24) Diagnostic analysis of fetal abnormalities Prenatal diagnosis Generic Generic