Consultancy- to develop an Electronic GMP Inspections System

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Introduction

Country:  Zimbabwe 

 

Description of the Assignment: Background The Medicines Control Authority of Zimbabwe (MCAZ) is a statutory body established under the Medicines and Allied Substances Control Act (MASCA) [Chapter 15.03], responsible for ensuring the safety, efficacy, and quality of medicines and allied substances in Zimbabwe. One of its critical functions is conducting Good Manufacturing Practices (GMP) inspections to assess compliance by manufacturers with local and international standards.

GMP inspections play a vital role in safeguarding public health by ensuring that medicines are consistently produced and controlled to the quality standards appropriate to their intended use. To strengthen its oversight and inspection capacity, MCAZ seeks the expertise of a qualified consultant to develop and implement GMP inspection protocols and tools aligned with WHO standards.

This increases transparency and availability of medical information in line with the best standards for WHO Global Benchmark Tool (GBT) Maturity Level 3 and 4. 

 

Period of assignment/services : 75 DAYS

 

Proposal should be submitted directly in the portal no later than indicated deadline.

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Documents :

Negotiation Document(s)
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