World Health Organisation Tender

Background Strengthening Regulation Of Medical Products Contributes In The Achievement Of Universal Health Coverage (uhc) By Ensuring The Quality, Safety And Efficacy Of Medical Products Before Being Used By The Public. Drug Product Registration Is The Process By Which A Country’s Regulatory Authority Assesses The Safety, Quality And Efficacy Of Medicines Available To Its Citizens And Is Key In Protecting Public Health. Fiji Mra Assessment Following Who’s Global Benchmarking Tool (gbt) Highlighted Product Registration As A Priority Area Of Action And In Need For Support. The Fiji Mra Has Been Preparing To Set Up Its Drug Registration Program Over The Years, However, There Is Still A Need To Support Capacity Building Activities For Fiji Mra Staff In This Area And Make The Organization Able To Develop And Start Its Own Registration System.   Purpose/specific Objective Of The Activity Review Current Legislation For Medical Products’ Registration In Fiji And Develop An Implementation Plan, Including A Product Registration Guideline, Sops, List Of Registered Products, Training Material And Further Recommendations To Fiji Medicines Regulatory Authority (mra)   Description Of Activities To Be Carried Out The Selected Consultant Is Expected To Work With In Collaboration With Who Division Of Pacific Technical Support (dps) And Fiji Medicines Regulatory Authority By: - desk Review Of Pertaining Legislation And Regulation For Medical Products In Fiji; - discuss The Results Of The Assessment With Who Dps, Fiji Nra And Ministry Of Health And Medical Services (mhms) And Provide Recommendations On The Way Forward; - develop An Implementation Plan For Drug Registration That Will Include Guidelines, Sops, Training Materials, Etc. - support Training Activities Of Fiji Nra Staff (office Of The Chief Pharmacist And Fiji Nra Personnel)   Methods To Carry Out The Activity Output 1: Implementation Plan Deliverable 1.1: Legislation Review And Writing Of Assessment Report On Drug Registration System Deliverable 1.2: Implementation Plan On Drug Registration Activities And Recommendations, Together With Supportive Documentation Such As Guidelines For Product Registration, Sops And Working Instructions, Hr Plan, Calendar Timeframes, Etc.   Qualifications & Experience Education Essential:  University Degree In Pharmacy Or Other Medical Sciences. Desirable: Postgraduate Qualification (msc Or Phd) In Pharmaceutical Legislation, Or Regulatory Affairs; Regulatory Affairs Professional Society Certification (rac) Will Be Considered   Experience Essential: Minimum Of Seven Years Of Experience In Pharmaceutical And Medical Products Regulation, Especially In Supporting Initial Marketing Authorization (product Registration) At International Level And Experience In Working In The Area Of Regulatory Convergence And Cooperation. Desirable: Experience Working With National Regulatory Authorities In Lmic And Small Island Developing States (sids)   Technical Skills & Knowledge Demonstrated Expertise And Good Knowledge On Pharmaceutical Regulatory System And Framework; Experience Supporting And Providing Guidance To Drug Registration Activities In Resource-limited Contexts; Good Interpersonal Skills And Capable Of Facilitating Discussion And Teamwork And Good Analytical Thinking And Writing Skills. Desirable: Experience Working In The Pacific Or, At Least, In Sids.   Languages Fluent In English   Competencies Teamwork, Respecting And Promoting Individual And Cultural Differences, Communication, Knowing And Managing Yourself And Producing Results.   Additional Information: Duration Of Contract: September – December 2021   Applications Qualified And Interested Specialists Should Submit Their Cv {for Individual Contractors} Or Company Profile {for Institutional Applications} And Expression Of Interest {cover Letter} To The Supply Officer Through Wp Ro Ungm At < Wproungm@who.int > By 19 August 2021.  The Cover Letter Should Outline How Their Experience And Qualifications Make Them A Suitable Candidate For This Position And Should Include Their Proposed Daily Consultancy Fee And Availability. Please Use Tender Notice No. 137088 As Subject To All Submission. Only Successful Candidates Will Be Contacted.