E-Learning
E-learning is the new wave for delivering training online and on demand using web-based technology. E-learning is a cost-effective way to participate in training with the option of 24/7 delivery. MTAA in association with SeerPharma, is pleased to offer a new and innovative online Medical Devices (MD) Regulatory and Quality e-learning series. The MD series is specifically designed for professionals within the medical technology industry.
Medical Devices (MD) Regulatory and Quality E-learning DISCover Series
Each module provides up to 45 minutes of interactive online training, links to supporting information, online assessments and a Certificate of Completion. Individual training records are stored on a secure Learning Management System (LMS) for later reference by users. This LMS is managed by SeerPharma.
The DISCover Series has been developed by industry experts and covers regulatory compliance to all major international cGMPs such as FDA, EU, PIC/s, TGA and ISO 13485/CFR 820. DISCover modules combine the impact of expert content and multimedia to make the learning experience simple, consistent, more engaging and more memorable. This program delivers best-practice and effective e-learning to the workplace.
The Modules
Understanding regulatory and quality requirements are integral parts of managing a medical device operation. This MD series has been designed to support and enhance industry professionals responsible for compliance and quality. Effective training has proven to enhance compliance, minimise failure and improve productivity. More modules are in production.
Registration
A range of online training options are available for MTAA members and non-members. To view more information about a module that interests you, please click on the link below. To register for a stand-alone module or a series of training, please call Ari Maidenberg, E-learning Manager, SeerPharma (+613 9897 1990).
Click on the link and register to engage in a stand-alone module or a series of training. A range of online training options are available for MTAA members and non-members.
MD-G 1: Global Regulation of Medical Devices
MD-G 2: Quality Management Systems - Requirements
MD-A 1: Australian Regulatory Affairs Overview
MD-A 2: Requirements for Registration
MD-U 1: USA Regulatory Affairs Overview
MD-U 2: Quality Systems Requirements - 21 CFR 820
MD-U3: US 510(k) Premarket Notification Scheme
MD-Q 1: Managing a Quality Management System (QMS)
