Summary
मेडिकल डिवाइस नियमों में ढील दी गई है, जिसमें आउटसोर्स स्टेरिलाइजेशन के प्रावधान शामिल हैं और EU को सख्त नियामक क्षेत्राधिकारों में जोड़ा गया है। इन संशोधनों का उद्देश्य नियामक आवश्यकताओं को सरल बनाना और पात्र चिकित्सा उपकरणों के लिए बाजार पहुंच को तेज करना है।
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