The Benefits of Achieving ISO 13485 Certification for Your Medical Device Business in the UK
Introduction ISO 13485 certification is a crucial step for any medical device business in the UK. It indicates compliance with international standards for quality management systems (QMS) tailored to the medical device sector, ensuring consistent adherence to customer and regulatory demands. This certification offers...
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(PMS) Post-Market Surveillance for medical devices is a regulatory requirement. It is mandatory in global markets including the United States and European Union. PMS comprises of activities that relies on data gathering....