A vaccine for CoViD is
getting much attention. There are
several firms in different countries working on it. Now there are articles on a macro view of the
number of planes needed to transport and the required temperatures for a
vaccine. These and other articles are interesting with their high-level view.
But they are not
actionable. What is needed is an end-to-end
(E2E) global supply chain operation plan to distribute the vaccine across the
world. This is complex in what must be
done, the geographic scope, product requirements, and the time pressure to do
it.
With a world population
of 7.8 billion and possibly 2 doses per person, this is a huge undertaking to
move it around the globe. Upfront, the
availability of potential transportation and storage resources seems
insufficient. That adds to the challenge
and need for a plan—to be ahead of the game and to minimize as many
problems—and there will be problems.
Presented here is a plan,
rough perhaps, with many unknowns at this time.
It is a working document that can be updated as more details/information
arises as to product requirements, production location or locations; country demand;
transportation, storage, and logistics resources; and other specifics evolve.
Please note, the names of any transportation, warehouse, or logistics firms
will not be mentioned. This is about the plan. Names will arise with the design
and implementation.
A very important
point. This project defines
VUCA—volatility, uncertainty, complexity, and ambiguity. The standard
approaches will not work. Change will be
a dynamic constant to the point it could be considered organized chaos.
Again, 7.8 billion people in 100+ countries, possibly 2 doses each, a potential vaccine that requires temperature protection at below freezing temperatures or face vaccine degradation. Protecting the vaccine from manufacturing through to injection is the underlying concern with the project and will require more than transportation and storage. VUCA. A project that defines challenge.
·
Prepare a list of contacts at receiving
countries who will coordinate, both medical and supply chain. Collaboration is
important for such an end-to-end undertaking.
·
Err on the side of caution with developing
and implementing the plan.
·
Start with vaccine raw materials/ingredients
(active and inactive)—where sourced, production rates and quantities, how to
ship, what is required for handling & storage, including space. Do not forget vials and/or ampules, caps,
labels, and packaging.
·
Understand production batch/lot sizes and
production rate, including any as to language for labels.
·
Establish a plan that covers the entire
timeline--from launch period through to expected production to satisfy worldwide
needs.
·
Know the product distribution plan—ship
how many to where and the sequencing/prioritization. That is a starting point. With this is recognizing how to pack the shipment to maintain temperature.
·
Measure time from door-to-door for each
origin-destination. This is critical for
product temperature protection.
·
Understand that transportation space and
availability and cold chain storage space will influence shipment sizes.
· Track vaccine drawdowns. This is important for shipment scheduling and to not have more product at a destination than there is temperature protection space.
·
Recognize destination and
origin-destination differences. This is not a one-size-fits-all approach. It
must understand and adapt to the product and operating realities. This is important.
·
Assign countries to ship to if there are
multiple production sites.
·
Collaborate and coordinate with
destination supply chain people on transport and warehouse issues, space, local
nuances, providers, and other issues.
This should be ongoing.
·
Determine special needs as to cold chain
and/or cool chain temperature for storage, transport, sanitary, chain of
custody. Do this for each tier of transport and storage for vials unopened and
opened. Chain of custody is important to
manage the product requirements, operational events, and to prevent criminals from
theft, and to restrict counterfeits.
·
Analyze space and service needs for air
cargo and cold/cool chain storage.
·
Calculate for each destination as to
shipments sizes, ready release dates, and the number of shipments.
·
Calculate storage needs at the origin,
including production rate and build inventory timing and releases/drawdowns.
·
Calculate storage needs for each
destination.
·
Focus on door-to-door speed.
·
Minimize the number of handlings, stops,
and transfers of products to mitigate temperature and contamination problems.
·
Understand destinations—airports, adequacies
for storage and moving vaccine safely.
·
Define what carriers, warehouses, and
transport/logistics providers can do as to product requirements, shipment/storage
over the total timeframe, and sanitary conditions. Do it for origin,
destinations, and intermediate locations.
·
Secure contractual firm space and service
commitments by origin-destination (not by an aggregate or macro basis) to meet
what is required for product requirements and time to perform, including
variation, for transport and warehousing.
Lock it up.
·
Conclude transport and storage
capabilities with production and distribution plans.
·
Set the technology to follow the movement
of the vaccine—bar code, RFID, or other.
·
Maintain temperature integrity. Track
end-to-end temperature.
·
Monitor chain of custody.
·
Achieve maximum E2E visibility,
technologies, and technology integration.
·
Understand Customs requirements at
destination airports to speed movement and quick handling from planes landing
and shipping to end destinations.
·
Quantify that hospitals, doctors, and
other medical/pharmaceutical places that will dispense vaccine can handle for
safe handling and storage.
·
Ensure needed supplies of syringes, swabs,
bandaids, gloves, and other needed PPE at each dispensing destination location.
The above would present
the ideal, Plan A model. But the best-laid
plans, including expected shortages of air cargo and cold chain storage
infrastructure and capabilities and stability, a Plan B, a C, and even D or
more to have the needed scope and viability, are useful to be ready for the
just-in-case and to cover all the needs, especially temperature related.
Here the purpose is to
identify, assess, and mitigate risks/problems. This would include:
ü Identify
areas/points where there are inadequacies, including destination alternatives
in the event of transport and/or storage shortcomings.
Analyze potential performance problem areas.
ü Review
ways to improve performance door-to-door and mitigate delays. Big ways to
lesser ways. For example, for customs clearance and freight payment.
ü Assess
gaps between needs and space availabilities.
ü Evaluate
technology gaps, such as for visibility.
ü Create
alternative lanes for transportation routes and storage for coverage.
ü Develop
cooling alternatives and how and where best to use them.
The plan that is
developed for the vaccine also has to be prepared for other events that can
affect the operations. For example, what
if there was a global demand surge for CoViD monoclonal antibody therapies that
would compete for many of the same supply chain resources as the vaccine?
There is much work to be done. Much is at stake here. And much to do it--the required process, technology, organization, and logistics infrastructure. A supply chain team in place early to design a program—then to manage it. The size and complexity of the project demand it.
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