Page 15 - Standard Operating Procedures (SOPs)
P. 15

GUIDELINES  ON  RESEARCH  ETHICS  AS  PER  NATIONAL  HEALTH
                    RESEARCH STRATEGIES:

                        ➢ The National Research Ethics Committee (NREC) will set   standards,  advice
                           the  Departments  and  the  Ministry  of  Health  &  Family  Welfare  on  the
                           management  of  research  ethics  for  Bangladesh  and  arbitrate  on  matters  of
                           Ethics.

                       ➢  The  NREC  will  be  responsible  to  review  all  clinical  trials  of  both  non
                           registered medicinal substances in Bangladesh and new indication of already
                           registered medicinal substances.

                       ➢  Research issues having religious or social sensitivity should be approved by
                           NREC

                        ➢ International collaborative research involving Bangladeshi  population   will
                           have to get ethical approval by the NREC, while the administrative approval
                           shall be given by the Government

                    Registration of Health Research as per National Health Research Strategy:

                           BMRC  has  developed  a  Registration  Form  for  registration  of  research
                           studies.  BMRC  is  developing  electronic  submission  system  for  health
                           research  registration.  There  is  a  specific  section  in  this  system  for  Clinical
                           Trial Registry.

                       ➢  Any health research to be conducted in Bangladesh has to be registered with
                           the BMRC.

                       ➢  The Clinical Trials Protocol should be reviewed and approved by the NREC.
                       ➢  Clinical  Trials  should  be  registered  in  the  Clinical  Trial  Registry  in  the
                           BMRC.
                       ➢  Clinical Trials be well monitored.

                       ➢  Clinical  Trials  should  be  conducted  following  ethical  standard  (Social  or
                           Scientific Value, Scientific Validity, Fair Subject Selection, Favorable Risk-
                           Benefit Ratio, Independent Review, Informed Consent & Respect for Potential
                           and Enrolled Subjects)
                           Clinical Trial

                       ➢  The NREC conducts post-approval monitoring of Clinical Trial.
                       ➢  It is mandatory to form Data Safety Monitoring Board (DSMB) for conducting
                           Clinical Trial.

                       ➢  At least 2 (two) members shall be included from NREC during formation of
                           DSMB.

                       ➢  Principal Investigator should report Serious Adverse Events (SAE) as well as
                           Adverse Events (AE) to the NREC.

                       ➢  Approval is given subject to several conditions.





                    SOP OF BMRC ETHICAL GUIDELINE                                                                                              Page 14
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