Page 21 - Ethical Guidelines for Conducting Research Studies Involving Human Subjects
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suggests an interest in a humane and civil  society, while on the other it
                          could  give  the  impression  of  experimentation  on  the  population  of  one
                          country by another. Different levels of development in terms of  intellectual
                          property rights etc; necessitate an ethical framework to guide   such
                          collaboration.  The  same  concerns  are  applicable  even  when  there  is  no
                          formal  collaboration  between  countries,  but  the  research  is  undertaken
                          with    assistance   from    international    organizations    as   sponsors
                          (Governmental like National Institutes of Health, USA, non-Governmental
                          like  Bill  &  Melinda  Gates  Foundation,  Ford  Foundation  or  others  like
                          WHO, UNICEF, UNAIDS, etc. ). (ICMR-2006)

                          Special Concerns

                          1.     Given  the  magnitude  and  severity  of  the  health  problems  in
                                 different countries, capacity building to address ethical issues that
                                 arise out of collaborative research must be promoted on a priority
                                 basis. Strategies should be implemented so that various countries
                                 and  communities  can  practice  meaningful  self-determination  in
                                 health  development  and  can  ensure  the  scientific  and  ethical
                                 conduct of research.

                          2.     The  collaborating  investigators,  institutions  and  countries  can
                                 function  as  equal  partners  with  sponsors  even  when  in  a
                                 vulnerable     position   by   building    appropriate    safeguards.
                                 Community representatives should be involved early enough while
                                 designing  the  protocol  and  in  a  sustained  manner  during  the
                                 development,  implementation,  monitoring  and  dissemination  of
                                 results of research.

                          3.     Careful consideration should be given to protect the dignity, safety
                                 and  welfare  of  the  participants  when  the  social  contexts  of  the
                                 proposed research can create foreseeable conditions for exploitation
                                 of  the  participants  or  increase  their  vulnerability  to  harm.  The
                                 steps  to  be  taken  to  overcome  these  should  be  described  and
                                 approval taken from NREC.

                          4.     Every  adult  participant  in  the  research  should  voluntarily  give
                                 informed consent and child her/his assent as may be applicable.

                          5.     As  different  kinds  of  research  (epidemiological  studies,  clinical
                                 trials, product development, behavioral and social science oriented
                                 research etc.) have their own particular scientific requirements and
                                 specific ethical challenges, the choice of study populations for each
                                 type of study should be justified in advance in scientific and ethical
                                 terms  regardless  of  the  place  from  where  the  study  population  is



                   BMRC ETHICAL GUIDELINE ON HUMAN SUBJECTS                                   Page 17
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