Achieving high uptake of COVID-19 vaccines will require effective planning, coordination, and implementation of a range of strategies. To assist, this toolkit offers a set of practical guidance, training and information resources that are intended to support programmes, partners, health workers, civil society organizations, and other stakeholders.
The toolkit is organized in line with the guidance on developing a National Deployment and Vaccination Plan (NDVP - UPDATED) for COVID-19 vaccines. The updated NDVP Guidance supersedes the previous version published on 16 November 2020.
COVAX other partners are working to ensure that the infrastructure, resources and technical assistance are available to help make sure that COVID-19 vaccines can be delivered to all those in need.
For questions, comments, or feedback, please email [email protected].
A National Deployment and Vaccination Plan is an operational plan to implement and monitor COVID-19 vaccination rollout in a country. The Vaccine Introduction Readiness Assessment Tool (VIRAT/VRAF 2.0) supports countries to assess readiness prior to introduction prioritize actions.
The 92 COVAX Facility Advance Market Commitment (AMC) countries must (and all other countries are welcome to) submit their COVID-19 National Deployment and Vaccination Plans (NDVPs) to be allocated vaccines through the COVAX Facility. NDVPs can be submitted by the designated national focal point through the COVID-19 Partners Platform. NDVPs will be reviewed by Regional Review Committees on a rolling basis to inform their recommendations on the allocation of vaccines by COVAX.
For countries:
The Infection prevention and control aide memoire is for policy makers, immunization programme managers, infection prevention and control (IPC) focal points at national, sub-national, and facility level, as well as for health workers involved in COVID-19 vaccination delivery. This document summarizes the key IPC principles to consider and the precautions to take for safely delivering COVID-19 vaccines.
WHO Prequalification aims to ensure medicines, vaccines and other health products for supply to low-income countries are quality-assured, safe, effective and accessible to all populations.
The WHO Emergency Use Listing Procedure (EUL) is a risk-based procedure for assessing and listing unlicensed vaccines, therapeutics and in vitro diagnostics with the ultimate aim of expediting the availability of these products to people affected
by a public health emergency.
For a vaccine to be procured through COVAX, it must be listed for emergency use by WHO through the EUL. EUL decisions and documents can also serve as a reference point for countries in their own regulatory decisions.
Vaccine-specific resources for COVID-19 vaccines that receive emergency use listing or prequalification. These resources are intended to support countries in preparing for COVID-19 vaccine introduction.
Following new vaccine introduction into a routine immunization programme, the purpose of a post-introduction vaccine evaluation (PIE) is to evaluate the impact of the vaccine introduction on the country’s immunization programme and to rapidly identify problems needing correction as vaccination expands in country.
The mini COVID-19 Post-Introduction Evaluation (mini-cPIE), also called the COVID-19 Vaccination Intra-Action Review (IAR), is a set of tools available to countries to review the early phase(s) of the roll-out of COVID-19 vaccine implementation. The mini-cPIE is a country-led facilitated discussion that aims to identify vaccine delivery challenges needing immediate corrective action and best practices for continual improvement and collective learning. The areas covered follow the National Deployment and Vaccination Plan for COVID-19 Vaccines (NDVP).
The mini-cPIE working documents (trigger question database, note taking template, and report template) are available here:
Countries are encouraged to begin using these working drafts for planning and implementation as needed. Given the evolving situation with the COVID-19 vaccine rollout, the trigger questions may be updated frequently based on feedback received. The mini-cPIE is recommended 2 to 6 months following COVID-19 vaccine introduction. Countries may adapt the questions as needed for their context.
This slide set provides an overview of how to conduct a mini COVID-19 Post Introduction Evaluation.
Watch the training recording: Mini-cPIE (COVID-19 Vaccination IAR) – What is it and how to conduct one?
Vaccine effectiveness and impact studies are needed to understand how the vaccine works in the real world. Guidance on how to conduct such studies, sample protocols, and other resources can be found here.
WHO's 'Vaccines Explained' series features illustrated articles on vaccine development and distribution. Learn more about vaccines from the earliest of research stages to their rollout in countries. For information on specific vaccines, please see above vaccine specific resources section.
Read all the 'Vaccines Explained' series.