Page 81 - Ethical Guidelines for Conducting Research Studies Involving Human Subjects
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before sampling starts, particularly so for  group    specific
                                         research like genetic research;

                                   vii.  samples  obtained  for  archival  purposes  in  a  prospective
                                         study. (ICMR, 2006, India)

                                   b)    Secondary Use:

                                   Every  request  for  secondary  use  shall  be  examined  by  the
                                   NREC/IRB to ensure that:

                                   i.    the  proposed  use  does  not  transgress  the  original  consent
                                         given for the earlier study and the validity of the objectives
                                         of the new study;
                                   ii.   provisions  for  ensuring  anonymity  of  the  samples  for
                                         secondary use are stated;
                                   iii.  after anonymizing sample, results are not communicated to
                                         the donor;
                                   iv.   for postmortem uses of samples the permission of the next of
                                         kin,  legally  authorized  representative  should  be  obtained;
                                         and
                                   v.    waiver  of  consent  is  given  whenever  the  donor  is  not
                                         traceable or the sample is anonymized. (ICMR, 2006, India)


                                   c)    Other Use:

                                   1.    Any  researcher  who  intends  to  use  samples  from  a
                                         Repository  must  submit  a  Statement  of  Research  Intent,
                                         which  must  be  approved  by  the  Ethics  Committee  of  the
                                         Repository,  which  shall  be  responsible  for  determining
                                         whether  the  intended  research  is  consistent  with  the
                                         informed  consent  provided  by  the  donor,  and,  where
                                         applicable, of the group.
                                   2.    Unless  scientifically  essential,  the  Repository  must  not
                                         provide  to  an  individual  researcher  any  information  linked
                                         to the samples.  When linked information is to be provided,
                                         only  the  minimal  information  as  required  for  the  intended
                                         research shall be provided.

                                   3.    If  any  commercial  use  is  made  of  the  samples  in  the
                                         Repository, appropriate written benefit-sharing agreements,
                                         consistent  with  the  policies  stated  earlier,  must  be  jointly
                                         signed  by  the  donor,  sample  collector  and  Repository  in-
                                         charge. It is also desirable that community consultations are
                                         held  prior  to  collection  of  samples  to  be  stored  in  a
                                         Repository, and group consent is obtained before individual
                                         consent.

                                   4.    There should be appropriate Material Transfer Agreements
                                         with  the  Repository  for  depositing  samples  as  well  as  for



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