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Pushing the Envelope for Pre-sterilized Vials

<span id="hs_cos_wrapper_name" class="hs_cos_wrapper hs_cos_wrapper_meta_field hs_cos_wrapper_type_text" style="" data-hs-cos-general-type="meta_field" data-hs-cos-type="text" >Pushing the Envelope for Pre-sterilized Vials</span>

The market for ready-to-use (RTU) containers is growing at a rapid pace. Drug manufacturers benefit from reduced time-to-market and total cost of ownership (TCO), as well as increased flexibility and greater integrity of the drug product. At the same time, they are looking for the ideal process to transfer pre-sterilized vials into the fill-finish area of a filling line. In an industry-first series of experiments, machine manufacturer Syntegon and drug containment solutions supplier Stevanato Group have joined forces to investigate Vaporized Hydrogen Peroxide (VHP) decontamination. Markus Heinz from Syntegon and Fabio Bertacchini from Stevanato Group share first insights.

Why did you start this project in the first place?

Fabio Bertacchini, Product Management Director at Stevanato Group: We brought the insights of a drug containment solutions provider to the table. Together with Syntegon, our goal was to gather the missing data to help our customers navigate this complex topic. Their main concerns are: do traces of VHP penetrate the packaging during decontamination? Could the H2O2 residue in the vials compromise the quality of the final product?

What is the verdict according to your data?

Fabio Bertacchini: Firstly, we now have more information and data to underline that VHP decontamination is a method that can be applied successfully to pre-sterilized vials. Results show that H2O2 residues are lower with RTU vials compared to bulk vials. Secondly, we have not only proven that the experiment carried out in Syntegon works – we can now also replicate it using our customers’ products. The tests will help us to gather the relevant data and support pharmaceutical companies in their decision whether VHP decontamination for RTU transfer is the best method for both their products and their production.

How would a drug manufacturer know whether VHP is the ideal method?

Markus Heinz: In the end, everyone must find their own method. There is no “one-fits-all” solution. But with our long-term expertise in isolator technology and this new data we are convinced that our offer is ideally suited for small batch manufacturing. It minimizes downtime and caters to a very specific, but rising need. Now our job is to continue testing the method to explore its full potential – and to share our results with our joint customers.

Sounds like there is still more to come?

Fabio Bertacchini: Absolutely. The study only marks the starting point of a new era in fill-finish processes for RTU vials – and maybe even other drug containment solutions.

Markus Heinz: Together with Stevanato Group, we will keep our studies and the good news going to provide new solutions for our customers – stay tuned!

Stevanato Group
Stevanato Group

Stevanato Group is a leading global provider of drug containment, drug delivery, and diagnostic solutions to the pharmaceutical, biotechnology, and life sciences industries. The Group delivers an integrated, end-to-end portfolio of products, processes, and services that address customer needs across the entire drug life cycle at each of the development, clinical, and commercial stages.

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