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2005 Edition Report on Drug Administration Procedure & Practices ...

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Part II Procurement Secti<strong>on</strong>, CPO1. Receiving the Complaint1.1 The officer receiving the call must ensure the complaint form is received afterbeing notified by the instituti<strong>on</strong> initiating the complaint.1.2 The officer receive the complaint must acknowledge the complaint by return fax tothe initiating instituti<strong>on</strong> immediately.1.3 The Pharmacist (Procurement) or his delegate must follow up with the initiatinginstituti<strong>on</strong> to ensure full understanding of the nature of the complaint and receiptof relevant samples where appropriate.1.4 Open case file which must be endorsed by Senior Pharmacist (Procurement) andcirculate within the procurement secti<strong>on</strong>.1.5 The report form must be used to document and communicate with relevant partiesby fax <strong>on</strong> all the activities taken throughout the entire exercise.2. Immediate Acti<strong>on</strong>2.1 The Pharmacist (Procurement) will assess the situati<strong>on</strong> and seek endorsement fromSenior Pharmacist (Procurement) <strong>on</strong> the course of acti<strong>on</strong>s to be taken.2.2 Organise, arrange and document all evaluati<strong>on</strong> testing <strong>on</strong> both the complaintsample and circulating stock respectively.2.3 Inform users, supplier, the Department of Health, the Government SuppliesDepartment and HA Central Procurement Unit if necessary <strong>on</strong> all acti<strong>on</strong>s taken asappropriate.2.4 Evaluate the situati<strong>on</strong> and make necessary arrangement to ensure c<strong>on</strong>tinuity ofsupply of the affected item if necessary.2.5 All acti<strong>on</strong>s and steps taken are properly documented <strong>on</strong> the report form.3. Follow-up Acti<strong>on</strong>3.1 Follow up <strong>on</strong> the progress of investigati<strong>on</strong> by supplier/manufacturer.3.2 Validate the outcome of the any investigati<strong>on</strong> by independent testing or c<strong>on</strong>sultexpert opini<strong>on</strong> where necessary.3.3 Assess the validity, accept or reject the submitted explanati<strong>on</strong> and proposedimprovements to be implemented by the supplier/manufacturer.3.4 Inform users, supplier, the Department of Health, the Government SuppliesDepartment and HA Central Procurement Unit if necessary <strong>on</strong> any proposedacti<strong>on</strong>s or recommendati<strong>on</strong> as appropriate.3.5 All acti<strong>on</strong>s and steps taken are properly documented <strong>on</strong> the report form.HAHO Aug 963

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