Policies
Department of Pharmaceutical Services
- Reporting Adverse Event Following Immunisation (AEFI) Guideline
- Annex II BruHIMS AEFI Reporting Form Quick Guide
- Guidance for Medicinal Product Defect, Quarantine and recall in non-Ministry of Health Facilities
- Best Practice Guidance: Good Antibiotic Prescribing Practice (GAPP)
- Guidance for Medicinal Product Defect, Quarantine and recall for licensed manufacturers/licensed wholesalers/licensed importers/ Product license holders in Brunei Darussalam
- Annex IV Product Recall Completion Form
- Guideline on Health Care Waste Management
- Brunei Darussalam Pharmacovigilance Guidelines
- Annex II Medicinal Product Defect Reporting From Licensed Manufacturer/ Licensed Wholesaler/ Licenced Importer/ Product Licence Holder To Ministry Of Health
- Annex III Medicinal Product Defect Form For Non Ministry Of Health Facilities To Licensed Wholesaler/ Licenced Importer/ Product Licence Holder
