Functional Areas
- Functional Areas
- Legal Framework
- Project Document
- The Grant Agreement
- UNDP-Global Fund Grant Regulations
- Grant Confirmation
- Grant Confirmation: Face Sheet
- Grant Confirmation: Conditions
- Grant Confirmation: Conditions Precedent (CP)
- Grant Confirmation: Special Conditions (SCs)
- Grant Confirmation: Limited Liability Clause
- Grant Confirmation: Schedule 1, Integrated Grant Description
- Grant Confirmation: Schedule 1, Performance Framework
- Grant Confirmation: Schedule 1, Summary Budget
- Implementation Letters and Performance Letters
- Agreements with Sub-recipients
- Agreements with Sub-sub-recipients
- Signing Legal Agreements and Requests for Disbursement
- Language of the Grant Agreement and other Legal Instruments
- Amending Legal Agreements
- Other Legal and Implementation Considerations
- Legal Framework for Other UNDP Support Roles
- Health Product Management
- Sub-recipient Management
- Capacity Development
- Interim Principal Recipient of Global Fund Grants
- A Strategic Approach to Capacity Development
- Resilience and Sustainability
- Legal and Policy Enabling Environment
- Functional Capacities
- Capacity Development and Transition
- Transition
- Capacity Development Objectives and Transition Milestones
- Capacity Development Results – Evidence From Country Experiences
- Capacity development and Transition Planning Process
- Capacity Development and Transition – Lessons Learned
- Risk Management
- Audit and Investigations
- Human Rights, key Populations and Gender
- Human Resources
- Legal Framework
Quality monitoring of health products
Quality monitoring of health products
According to the UNDP QA Policy and the Global Fund’s QA Policies, the quality of products procured through UNDP must be monitored throughout the supply chain.
To facilitate compliance with, and implementation of, the UNDP QA Policy, GFPHST has developed further Guidance for UNDP Country Offices on Health Products Quality Assurance in the Supply Chain, which includes a template for developing a QA Action Plan. This document provides UNDP COs with guidance on how to maintain and control the quality of health products in national supply chains, from the delivery point in country up to the end user, in collaboration with National Regulatory Authorities (NRA).
Quality monitoring of health products
Quality Monitoring at different stages
READ MORE
Quality monitoring of health products
Quality Control (QC) activities
READ MORE
Quality monitoring of health products
Surveillance and monitoring for substandard and falsified medical products
READ MORE
Resources
Functional Area: Health Product Management Project Stage: Grant Implementation Author: The Global Fund Language: English Type: Policies, Procedures and guidance Topic: QA Policies, Quality Control Measures, UNDP Quality Assurance Policy, Quality Assurance Resource File Format: Link Resource Accessibility: Publicly accessible