The new MDR (EU) 2017/745 brings about changes that will create new jobs as well! In this article, we will look into the new requirement of appointing a Person Responsible for Regulatory Compliance (PRRC).
Join us for a Live Webinar, hosted by Jason!
Organised with the Asia Regulatory Professional Association, we will be hosting a webinar on how companies can adopt standards with ease and automate QMS processes on the cloud. In this webinar session, we will be sharing on the common difficulties companies face and how we intend to tackle them directly!
Singapore Manufacturing Federation (SMF), in collaboration with Stendard, is bringing you a 2-day workshop. This workshop focuses on providing an overview of the ISO 13485:2016 and how these requirements can be continuously met using an Enterprise Quality Management Software System (EQMS). We will also be sharing how effective implementation of the standard can help companies fulfill medical device regulatory requirements globally.