Page 22 - Ethical Guidelines for Conducting Research Studies Involving Human Subjects
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selected.  Generally,  early  clinical  phases  of  research,  particularly
                                 of drugs, vaccines and devices, should be conducted in communities
                                 that are less vulnerable to harm or exploitation. However, for valid
                                 scientific  and  public  health  reasons,  if  sufficient  scientific  and
                                 ethical safeguards are ensured it may be   conducted in any phase
                                 after obtaining relevant regulatory clearances.

                          6.     The  nature,  magnitude,  and  probability  of  all  foreseeable  harms
                                 resulting from participation in a collaborative research programme
                                 should  be  specified  in  the  research  protocol  and  explained  to  the
                                 participants  as  fully  as  can  be  reasonably  done.  Moreover,  the
                                 modalities  by  which  to  address  these,  including  provision  for  the
                                 best  possible  nationally  available  care  to  participants  who
                                 experience  adverse  reactions  to  a  vaccine  or  drug  under  study,
                                 compensation  for  injury  related  to  the  research,  and  referral  for
                                 psychosocial and legal support if  necessary, need to be described.

                          7.     The  research  protocol  should  outline  the  benefits  that  persons  /
                                 communities  /  countries  participating  in  such  research  should
                                 experience as a result of their participation. Care should be taken
                                 so  that  these  are  not  presented  in  a  way  that  unduly  influences
                                 freedom  of  choice  in  participation.  The  burden  and  the  benefit
                                 should be equally borne by the collaborating countries.

                          8.     Guidelines,  rules,  regulations  and  cultural  sensitivities  of  all
                                 countries participating in collaborative research projects should be
                                 respected,  especially  by  researchers  in  the  host  country  and  the
                                 sponsor  country.  These  could  be  with  reference  to  intellectual
                                 property  rights,  exchange  of  biological  materials  (human,  animal,
                                 plant  or  microbial),  data  transfer,  security  issues,  and  issues  of
                                 socially or politically sensitive nature. (ICMR-2006)

                   08.    RESEARCHER’S  RELATIONS  WITH  THE  MEDIA  AND
                          PUBLICATION PRACTICES

                          Researchers  have  a  responsibility  to  make  sure  that  the  public  is
                          accurately  informed  about  results  without  raising  false  hopes  or
                          expectations.  It  should  also  not  unnecessarily  scare  the  people.
                          Researchers should take care to avoid talking with journalists or reporters
                          about  preliminary  findings  as  seemingly  promising  research  that
                          subsequently cannot be validated or could lead to misconcepts if reported
                          prematurely.  Or,  the  results  of  research  may  be  reported  in  such  a  way
                          that it would seem that the human application is round the corner, only to
                          be told later by the researchers that considerable time has to pass before
                          these  findings  can  be  translated  into  tools  for  human  use.  In  such




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