Page 78 - Ethical Guidelines for Conducting Research Studies Involving Human Subjects
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13.10  BIO-BANK

                          A biobank is  a  form  of biorepository devoted  for  storing  human  biological
                          samples include embryonic stem cells, neonatal tissues (Wharton’s Jelly ),
                          iPS cell lines, adult stem cell lines, sperm, ova etc. from large number of
                          individuals  intended  for  future  use  by  multiple  researchers  for  multiple
                          purposes.  Multiple  biobank  exist  in  the  developed  countries  and  some
                          developing  countries.  As  future  research  on  genomics,  personalized
                          medicine, cancer etc. will heavily depend on biorepository, it has invoked
                          research and medical ethical questions as well as national issues.

                          Types of biobank:

                          1.     Tissue  banks  harvest  and  store  human  tissue  from  living,
                                 cadaver and biomedical (pathological) samples.

                          2.     A virtual biobank is a virtual repository which provides         data
                                 extracted  from  and  characterizing  samples  stored  at  an
                                 existing biobank.

                          3.     Population  banks store  biomaterial  as  well  as  associated
                                 characteristics  such  as  lifestyle,  clinical,  and  environmental
                                 data.

                          The biorepository activities involve three components:


                          1.     Collection of tissue samples;

                          2.     The repository storage and data management; and
                          3.     The recipient investigators, type of research and its     outcome.
                                 (ICMR, 2006, India)


                          13.10.1 Repository Collections

                                 The  steps  involve  the  initial  process  of  collecting,  processing,
                                 freezing, “anonymizing”, and storing tissue with  its  corresponding
                                 clinical  information  in  a  database.  As  tissue  banking  concerns
                                 research  at  a  later  time,  the  ethical  issues  pertain  to  consent
                                 requirements for the banking and further uses of tissue and DNA
                                 samples, their control and ownership, and the benefit sharing to the
                                 individual or community. Permission must be obtained for shipping
                                 samples abroad.

                                 The sample collector must obtain informed consent of the donor for
                                 DNA  banking  or  for  cell-line  transformation  and  banking.    The
                                 process of seeking informed consent for purposes of banking must
                                 clearly  be  stated  in  addition  to  possible  risks  and  benefits,  the
                                 conditions  under  which  samples  from  the  Repository  shall  be
                                 provided to other researchers, how long and in what condition the




                   BMRC ETHICAL GUIDELINE ON HUMAN SUBJECTS                                   Page 74
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