This course is based on the 2016 version of the ISO 13485 Standard, providing skills necessary to perform internal process audits in the medical device industry. It features a detailed review of the ...

This course is based on the 2016 version of the ISO 13485 Standard, providing skills necessary to perform internal process audits in the medical device industry. It features a detailed review of the ...

In this two-day workshop, you will gain the knowledge and skills you need to audit your quality system to the ISO 13485:2016 standard. Course topics include updates the ISO 13485 standard, ISO ...

This webinar is intended to help you get familiar with how to establish an internal audit program of the quality management systems (QMS) for medical device manufacturers in preparation for an FDA ...

Medical device companies, listen up. There is zero excuse for not complying with medical device quality system regulations. FDA has published and makes available ALL regulations required for medical ...

Globally, the medical industry is continuously growing and is highly dependent on technological advancements and essential procedures aimed at producing the best treatments. To make sure proper ...

Continued ISO 27001, 27017, 27018, 13485, SOC 2 Type 2, and HITRUST Certification Reflects Ongoing Commitment to Trusted Health Data Management TORONTO, ON / ACCESS Newswire / August 7, 2025 / Smile ...