After we propose cold chain package designs for clients what happens next?
Let’s use the scenario where our pharma/bio client has now approved the cold chain package design proposed by our packaging engineering team. In this scenario, the initial testing showed the packaging’s performance meeting the target protection goals.
We are now positioned to move to official qualification testing for the proposed package design. This includes full reporting on all aspects of the package and testing procedures. The pharma/bio clients need this full cold chain package qualification reporting for their records. This information documents and proves to their clients and regulatory agencies that the packaging is properly designed and tested to adequately protect their vital healthcare products. When a life is potentially on the line, the packaging must be solid and proven.
Qualification testing can be performed by the in-house Integritemp thermal testing lab staff with full reporting capabilities. However, to avoid any appearance of conflicts of interest, clients will typically contract for qualification testing with an independent third-party testing lab.
We fully support and encourage third-party testing to obtain un-biased scientific data. Our staff will work closely with the third-party lab to supply all materials, designs, and testing requirements needed for the final qualification testing.
What happens next?? Stay tuned for next month’s blog! We continue our walk through the cold chain package design implementation process once qualification testing is complete.
Please watch for next month’s blog where I will continue our conversation with more facts, figures, and good news about EPS foam!
Greg Montgomery
gmontgomery@integritemp.com
Office: 402-884-4290