Overview
Learn more about how to optimize a quality management system to meet medical device regulatory requirements.
Ongoing global harmonization activities and proliferation of statutory quality management system (QMS) requirements for regulatory compliance are a tough terrain for medical device and IVD companies to navigate, Our webinar will help attendees develop a greater understanding of the decision points and strategies to consider when planning QMS upgrades to help your company comply with additional medical device market regulatory requirements.
The presenter will review various global QMS standards and regulations, including the Medical Device Single Audit Program (MDSAP), discuss key areas of impact and offer recommendations on how to optimize a QMS structure to simplify the upgrade process and allow for more efficient future updates to include additional applicable requirements.
Schedule
Date: 30 Jul 2024, Tuesday
Time: 11:00 PM - 11:45 PM (GMT +8:00) Kuala Lumpur, Singapore
Location: Online
