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LEARN FOR FREE The Digital Health landscape is rapidly expanding and innovating. In this webinar Peter Fitzgerald delivers an informative and interesting presentation of digital health in the COVID Age and forward. -
With the new Medical Device Regulation now in force as of 26 May 2021, Meditrial has organized this live event reserved for our customers and partners, to help you understand what changes impact you and manage the transition for ongoing and new clinical trials. Thus, this training will allow you a quick and rapid upgrade of your trials to the updated regulations according to MDR. -
This lecture describes the key changes regarding post market surveillance and what companies should do to meet their new obligations. After the course you can take a final test to receive your certification. Enjoy! -
This course describes key principles of general safety and performance requirements. In this video we will discuss in detail article 56 of IVDR and will give practical advices on how to plan and prepare for the IVDR. Finically, we will explain what is the performance evaluation and which periodic deliverables and when need to be updated accordingly. -
This lecture presents the new European regulation for medical devices and provides an easy to learn overview of all the key changes. Learn all you need to know for a successful transition to the new legislative framework. -
This video lecture discusses the impact of COVID-19 on clinical trials, potential pathways and modifications needed to run a successful trial and how new technologies can assist in moving forward. -
LEARN FOR FREE This course will cover some basic concepts to review the reimbursement system and define the role of health economics and outcomes research and will focus on how to incorporate health economics in the market access strategy. -
In this training, you will learn what IDE means, and how to prepare and submit your application to the FDA. -
The goal of this presentation is to provide you with the essential elements for success and to teach you how to apply the information to your project. Navigating the regulatory process and planning clinical trials can be the most daunting aspect of running your start-up. -
This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
