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Complaints received from the patients or patients’ representative were dealt according to the patient
             grievance mechanism plan, as stipulated under Act 586. There were complaints warranted investigations
             to be carried out such as complaints that were received from other parties and complaints that involved
             death of the patient or other detrimental issues, following which necessary actions will be taken in
             accordance to Act 586 such as show cause notice, suspension or revocation of Licence or Registration.


                                                     Figure 24
                     Number of Complaint Handling Mechanism for Complaints Received in 2017


               250
                                    222
               200
                                                                        143
               150

               100
                                                                                     No. of complaints
                50

                 0
                          Grievance Mechanism Plan                  Investigation

             Source: Private Medical Practice Control Section, MoH

             7.  Quality Unit
             The scopes and functions of Quality Unit are:
             i.   To handle case related to notification of incident reporting;
             ii.  To handle case related to notification of assessable death;
             iii.  To handle statistic summary unforeseeable or unanticipated incidents (incident reporting (IR-2A
                 dan IR-2B)
             iv.  To investigate maternal mortality and under 5 mortality involving PHFS; and
             v.  To coordinate establishment Jawatankuasa Penilaian Kematian Kebangsaan(JPKK) for asessable
                 death.


             Enforced since 1 January 2011, all licensed facilities under Act 586 were required to report their
             unexpected incidents (Incident Reporting - IR) and occurrence of Assessable Death (AD), as directed
             under Director General of Health’s Directives No. 1/2010. The aim of monitoring these IR and AD are
             mainly for the purpose of quality improvement. All reporting and notifications will not be subjected to
             punitive action.

             The scope of IR and AD is mainly to gather data and information regarding incidents and deaths that
             occurred in PHFS. The reporting and notifications are on voluntary basis, using these forms:
             i.   Form IR-1  : every time any incident (as listed in form) happen;
             ii.  Form IR-2  : 6-months statistical summary of incidents that occur (incidents that are not listed to
                 be reported under IR-1);
             iii.  Form AD-1: every time an assessable death occurs (within 72 hours of death).







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