considering sterilization in the design phase

Sterilization is not just a manufacturing step—it starts in the design phase. Planning for it early saves time and reduces costs. Here are four aspects to consider that can make a BIG difference in your design process, and beyond…

1️⃣ The Sterilization Chamber: Learning about the usable dimensions of the sterilization chamber while your design is still flexible can allow you optimize your use of the chamber. This allows you to process more devices at once, and make the most of each sterilization run.

2️⃣ Sample Requirements: Don’t wait until its time to start the sterilization validation to consider how many devices will be consumed in the process. A quick discussion with the sterilization specialist will help you know what to expect, and how to be prepared.

3️⃣ Packaging and logistics: Different sterilization facilities have different capabilities when it comes to receiving and processing your devices. Understanding what your sterilization provider can and cannot do might impact how, when, and where you package your device.

4️⃣ R&D sample generation: Biocompatibility testing, packaging validation, and other design activities all require quick access to sample devices that have been exposed to the entire manufacturing process. Can your sterilization provider quickly process a small amount of samples when you need them?

MASS-EO’s commitment to communication and customer service ensures that you’re informed as possible, from the start of your process, to the end, and beyond.