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
Global Data Standards
Global Data Standards
To improve traceability and end-to-end visibility of health products throughout the supply chain, to enhance efficiency, security and patient safety, and, ultimately, to improve the availability of health products at service delivery level, UNDP has adopted GS1 Guidelines for Global Health Commodities for product identification, location identification, and product master data.
UNDP, in collaboration with key stakeholders, is introducing GS1 standards as part of its procurement requirements and will support country uptake of these standards to improve tracking and traceability systems. These include the requirements that:
- Distribution and inventory management systems include a mechanism to trace, by batch number, the patients to whom medicines are distributed, in the event that a product is recalled; and
- All storage facilities and personnel use the ‘first expired, first out’ (FEFO) system.
Resources
Functional Area: Health Product Management Project Stage: Grant Implementation Author: USAID Language: English Type: Policies, Procedures and guidance Topic: Global Health Commodities, Procurement, Logistics Resource File Format: Link Resource Accessibility: Publicly accessible