{"id":1184,"date":"2014-02-18T19:33:10","date_gmt":"2014-02-19T03:33:10","guid":{"rendered":"https:\/\/blogs.plm.automation.siemens.com\/t5\/Polarion-Blog\/Leverage-ALM-for-Medical-Regulatory-Compliance\/ba-p\/380829"},"modified":"2026-03-26T05:35:42","modified_gmt":"2026-03-26T09:35:42","slug":"leverage-alm-for-medical-regulatory-compliance","status":"publish","type":"post","link":"https:\/\/blogs.sw.siemens.com\/polarion\/leverage-alm-for-medical-regulatory-compliance\/","title":{"rendered":"Leverage ALM for Medical Regulatory Compliance"},"content":{"rendered":"

Last week I moderated a webinar titled Using Software in Regulated Medical Environments<\/EM> in which Griffin Jones and Jamie Cole, global experts<\/STRONG> in medical device<\/STRONG> and software regulatory<\/STRONG> issues, shared their thoughts and experiences. The format was informal with lots ofattendee engagement. A key topic of interest was on ALM software<\/STRONG> and the benefits surrounding the implementation while attempting to meet regulatory requirements such as the FDA\u2019s General Principles of Software Validation.<\/A><\/p>\n

It was interesting to get a non-vendor perspective<\/STRONG> as to the importance of a) choosing the correct ALM solution and b) how ALM software is actually used for managing and helping companies achieve regulatory compliance. It was gratifying to hear that our solutions play a key role in achieving compliance. On behalf of the entire Polarion Software community, thank you Griffin and Jamie for a super presentation.
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Watch this 5-minute preview here:<\/P><\/p>\n