Sterilization Standards for Medical Devices in Oman – Regulatory Guide

 Sterilization is a critical step in ensuring the safety and effectiveness of medical devices in Oman. This guide explains the key sterilization standards, ISO compliance requirements, and Ministry of Health (MOH) regulations that every manufacturer must follow. From choosing the right sterilization method to meeting international quality benchmarks, manufacturers can avoid delays and ensure product safety. Operon Strategist provides expert consulting, turnkey project support, and regulatory guidance to help medical device companies in Oman achieve compliance and gain faster market approvals.


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