Products/Services
Type
Country
Country
Status
Completed
Product/Service
Clearly establish criteria and subsequently identify regulatory functions that can be carried out at country level and those which can be best undertaken through a sub-regional regulatory platform.
Deliverables
A white paper detailing rationale, feasibility and (if appropriate) road map for establishing a sub-regional approach to parts of the medicine and vaccine regulation processes.
Technical Areas
Pharma and Medical Products
Programme Implementation
0
GPW
GPW 13
GPW Output
1.3.3 Country and regional regulatory capacity strengthened, and supply of quality-assured and safe health products improved, including through prequalification services
GPW Outcome
1.3 Improved access to essential medicines, vaccines, diagnostics and devices for primary health care
Dates
to