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ALLpaQ awarded the prestigious King's Award for Enterprise In International Trade
As a leading manufacturer in the packaging industry, we are honoured that ALLpaQ have been awarded with the prestigious King’s […]
Dec 05th, 2024
ALLpaQ awarded the prestigious King's Award for Enterprise In International Trade
Dec 05th, 2024
Vaccine development has been vital in combating some of the world’s most infectious diseases, from measles and rubella to influenza and coronaviruses.
In order to keep the general public immunised against such diseases, companies within the biopharmaceutical industry must follow stringent cold-chain vaccine transportation processes to ensure vaccine production is efficient, safe and consistent.
Throughout this blog, we investigate cold chain vaccine transportation in-depth and the importance of bioprocess containers within vaccine development.
Cold chain vaccine transportation refers to the safe movement of biomanufacturing fluids from facility to facility – a crucial stage within the wider cold chain management process.
A significant element of cold chain vaccine transportation involves keeping vaccines stored as intermediates at their optimal temperature throughout the entire manufacturing cycle.
Maintaining safe temperatures throughout the vaccine manufacturing process helps to ensure an effective vaccine at the point of patient administration.
Temperature control after vaccine production is essential in the biopharmaceutical industry for various crucial reasons:
Vaccines are sensitive biological substances easily impacted by temperatures or fluxes in temperature. Producing and housing vaccines at the incorrect temperature can change their biological composition, ultimately reducing potency.
For example, the MMR vaccine, like most others, should be kept within the 2°C-8°C temperature range, and away from direct light.
Furthermore, large molecule types including the mRNA vaccine have even more unique cold chain requirements and must be stored according to their biological requirements.
A failed vaccine can lead to significant risks such as unsafe products and ineffective immune responses to disease, which leaves vulnerable lives in danger.
Consequently, it could even create doubts about the effectiveness of vaccines, influencing patients to avoid future vaccinations altogether, and causing a spike in infection rates.
An unstable vaccine supply can create a lack of trust in the manufacturer from a consumer standpoint, who may even terminate your supply contract and award it to another company in the vaccine industry.
Given that healthcare providers run on efficiency, trying to win back their trust would be exceedingly difficult, so it’s best to ensure your processes are carefully monitored, and efficient production is maintained.
Temperature excursions that cause unfit-for-purpose vaccines ultimately result in wastage and lost profit. With enhanced cold chain management, resources, employee time and transportation costs aren’t needlessly squandered, and profit margins aren’t negatively impacted.
During the vaccine development process, it’s typically the manufacturer’s responsibility to ensure vaccinations are kept in temperature-controlled environments before distribution.
Biomanufacturing facilities follow strict vaccine storage procedures and utilise modern equipment to protect fluids from temperature excursions, contamination and impact damage.
Such technologies include bioprocess containers designed to house single-use bags.
The integrity of single-use bags can be impacted by temperature variations and physical impacts during storage and transport, resulting in leakages that lead to contamination and wastage.
With this in mind, fluid transportation depends on effective and reliable storage equipment, such as bioprocess containers, which are used to store and transport vaccine materials throughout manufacturing.
Bioprocess containers are traditionally single-use technologies crafted from foldable film and poly materials that house primary packaging, specifically single-use bags containing vaccine solutions.
Yet, while these structures eliminate the need for post-cleaning, they aren’t the most durable and don’t help businesses in their quest for sustainability.
This differs greatly from a reusable hard plastic polyethene bioprocess container from ALLpaQ designed to rapidly transform your laboratory operations for the better.
Why choose ALLpaQ containers?
ALLpaQ foldable bioprocess containers have revolutionised biopharmaceutical vaccine handling and storage. In addition to maintaining cold chain stability during vaccine storage and movement, ALLpaQ systems are reusable and offer additional ecological and cost-saving benefits, unlike single-use containers.
With our robust plastic vaccine storage and distribution systems, you can fully trust that your biological products maintain their efficacy throughout the manufacturing process.
This is thanks to their extreme durability and strength properties that shield media from impacts during transit, optimal temperatures are maintained and the likelihood of bag tears is reduced significantly.
Additionally, the potential for contamination is greatly reduced thanks to smooth jet washable surfaces for easy cleaning.
Other advantages include:
Eager to revolutionise your current biological storage laboratory systems? If so, you’ve come to the right place.
At ALLpaQ, we’re experienced manufacturers of bioprocess containers trusted by clients and partners in over 25 countries worldwide.
Our expert team can assess your particular bioprocessing requirements and help you choose a bioprocess container that meets your needs.
To find out more, contact a member of our team online or call us on 01472 800 373.