{"id":5233,"date":"2023-01-31T11:52:45","date_gmt":"2023-01-31T11:52:45","guid":{"rendered":"https:\/\/www.imsm.com\/philippines\/?p=5233"},"modified":"2023-01-31T11:52:45","modified_gmt":"2023-01-31T11:52:45","slug":"how-do-i-get-iso-13485-certification","status":"publish","type":"post","link":"https:\/\/www.imsm.com\/philippines\/news\/how-do-i-get-iso-13485-certification\/","title":{"rendered":"How do I get ISO 13485 certification?"},"content":{"rendered":"
If you’re a medical device manufacturer, it’s likely that ISO 13485<\/a> will be on your radar. This internationally-recognised standard ensures such vital technology as yours is safe, effective and delivered to a high quality. Not only does the certification help you becom compliant with national and international legal requirements, but it will also help you to open your business to a global market. Here’s how to become ISO 13485<\/a> certified.<\/p>\n ISO 13485<\/a> is a type of quality management system for organisations that provide medical devices. Anyone in the industry knows that your product needs to consistently meet client and regulatory requirements.<\/p>\n ISO 13485<\/a> is the most accepted global standard of its kind and comes with a wealth of advantages. The benefits of ISO 13485<\/a> include:<\/p>\n In a nutshell, no, ISO 13485<\/a> is not mandatory, however, certification is extremely important as it harmonises your practices with legal and regulatory requirements that exist across the country, the EU and the rest of the globe. While not mandatory, an organisation may find difficulty operating in some markets or getting their product recognised without it. Like most ISO standards, the framework is flexible, and you can build a QMS for medical devices that suit your organisation as long as it meets international standards.<\/p>\n Many medical device manufacturers find that expert consultants can help them implement their ISO 13485<\/a> QMS with ease. With IMSM, our consultants work with you to design your QMS and design control requirements, before submitting your organisation to a recognised certification body to audit your business and get you ISO 13485<\/a> certified.<\/p>\n ISO 13485<\/a> requirements are applicable to any organisation, no matter the size or complexity, including services as well as products. The structure of the standard consists of eight sections: the first three are introductory, and the final five contain details of the requirements for compliance for medical device manufacturing. The five main sections are as follows:<\/p>\n The next step involves operating your newly-implemented QMS so you can collect the necessary documentation to audit, review your system and receive certification. These steps are as follows:<\/p>\n Download our free guide<\/a> to ISO 13485<\/a> now and find out more about the standard and the certification process.<\/p>\nWhat is ISO 13485?<\/h2>\n
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Is ISO 13485 mandatory?<\/h2>\n
How to get ISO 13485 certification?<\/h2>\n
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