3 Ways to Streamline Your Packaging Validation Process
When it comes to medical device manufacturing, validation is a critical step to ensure compliance, safety, and efficiency. However, it can also be a time-consuming and resource-intensive process. At Cretex Medical | QTS, we understand these challenges and have developed innovative solutions to help streamline your validation process without compromising quality or compliance.
January 21, 2025
Cretex Medical | QTS can help you streamline your validation process with QSEAL, QSTERILE and our Stock Package Program.
When it comes to medical device manufacturing, validation is a critical step to ensure compliance, safety, and efficiency. However, it can also be a time-consuming and resource-intensive process. At Cretex Medical | QTS, we understand these challenges and have developed innovative solutions to help streamline your validation process without compromising quality or compliance. Here are three key ways we can help:
1. Utilizing QSEAL: Pre-Validated Packaging
Validation of sterile barriers can be complex and costly. That’s why we’ve developed QSEAL, designed to provide consistent and reliable results. QSEAL is supported by rigorous testing and validation protocols, making it an ideal choice for medical device manufacturers looking to simplify their project timeline. By leveraging QSEAL, you can reduce time spent on repetitive validations while ensuring your products meet stringent industry standards.
2. Leveraging Our Stock Package Program
The lead time on packaging materials to start your project validations can be extensive. To ease this burden, QTS offers a stock package program featuring pre-validated packaging solutions. Our program includes a variety of packaging configurations designed to meet diverse needs, eliminating the need for custom packaging validations. By utilizing our stock packages, you can save time, reduce costs, and get your products to market faster, all while maintaining the highest quality standards.
3. QSTERILE: EO Pre-Validated Cycle
Sterilization validation is often one of the most time-intensive aspects of medical device manufacturing. With QSTERILE, our EO pre-validated sterilization cycle, you can significantly reduce the time and complexity associated with this critical step. QSTERILE is designed to accommodate a wide range of product types and sizes, allowing for faster onboarding and validation. By leveraging QSTERILE, you can focus your resources on other areas of product development while ensuring effective and compliant sterilization.
At Cretex Medical | QTS, we are committed to helping our customers overcome validation challenges through innovative solutions and expert support. Whether you’re a startup navigating the validation process for the first time or an established manufacturer looking to optimize your operations, our team is here to help. Contact us today to learn more about how our QSEAL, stock package program and QSTERILE solutions can streamline your validation process and accelerate your path to market.
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