I offer specialized consultation services for ISO 13485, Malaysia GDPMD, and Singapore GDPMDS compliance. With a thorough understanding of the regulatory landscape, I guide medical device manufacturers in achieving and maintaining quality management systems that meet international standards. My services include tailored assessments, documentation support, and training to ensure your organization is fully compliant with the necessary regulations. Together, we can streamline your processes, enhance product quality, and facilitate successful market access in the European Union, Malaysia and Singapore.