The introduction of new EU pharmacovigilance legislation presents opportunities in risk-based audits, QMS, and compliance improvement across regulatory activities. Training courses support ...

The ISO 13485:2016 training course presents a key market opportunity for medical device organizations to enhance their quality management systems, ensuring compliance with industry and regulatory ...

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 ...

Digital outdoor media leader QMS today announced a series of key appointments across its Strategy division, as it accelerates investment in its strategic capability to drive further innovation and ...

Over the years, HGI's work has received attention from press release platforms, trade publications, industry review outlets, ...

This article is brought to you by our exclusive subscriber partnership with our sister title USA Today, and has been written by our American colleagues. It does not necessarily reflect the view of The ...