Compliance shouldn’t be a reactive scramble. It should be a proactive strategy. 🛡️
When the new ISO 11137-1:2025 revision was released, GRAND TEN HOLDINGS SDN BHD didn’t hesitate. They partnered with us at ARG Academy to ensure their team was “ever-ready” to adopt the latest requirements.
Over two intensive days, we had the privilege of training 13 of their top professionals. The engagement was incredible.
We didn’t just cover the basics. We dug deep into the gritty, real-world applications of sterilization for healthcare products, unpacking:
🔹 The critical gaps between the 2006 (+Amd 1:2013) and 2025 revisions.
🔹 The “why” and “how” behind dosimeter uncertainty calculations.
🔹 Corrective action protocols for routine bioburden and dose audit failures.
🔹 Navigating compliance when modifying a product or sterile packaging system.
When a company invests this heavily in understanding the nuances of standard requirements, it speaks volumes about their commitment to quality and patient safety.
Thank you, Grand Ten Holdings, for trusting ARG Academy to guide you through this transition!
To our QA and RA connections: Which of the 4 topics above is currently your top priority?
Is your QA team prepared for the ISO 11137-1:2025 changes? 🚨
Don’t wait for a compliance gap. We have lots of sterilization training available.
Click button below & send us enquiry for the training.