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In this course, you will learn all the important information about the CTIS, its timelines and user roles. You’ll also discover what training materials are available at European Medicines Agency website. -
Pharmacovigilance is required through the entire life cycle of a drug – starting from preclinical development stage, going through continues monitoring till regulatory approval as well as spanning post-market stidues. Discover with Meditrial all aspects of European Pharmacovigilance and Drug Safety that include collecting, analyzing, monitoring, and preventing adverse effects in new drugs and therapies. Upon completing a course, you will take a final test to receive a digital certificate that can be printed. -
Discover the world of innovation and medical standards made easy, learn about the brand new ISO 22679 draft standard for cardiac occluders. -
The shortage of personal protective devices has endangered countless lives of healthcare operators working in COVID-19 treatment facilities. This is a widespread and prevalent issue worldwide. After the course, you can take a brief 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. -
Discover the world of innovation and medical standards made easy, learn about the brand new ISO 22679 draft standard for cardiac occluders. -
LEARN FOR FREE
Stiamo attraversando la fase 2, ma la fase 3, la fase della Consapevolezza della Nuova Normalità, sarà quella decisiva per molti aspetti, per il lavoro, l'economia, la salvaguardia della salute, la sicurezza. Inizia a farsi chiaro che sono e saranno molteplici le insidie nell'ambito della mental health che i nuovi scenari stanno già sollecitando oggi. Parleremo di come prepararci ad affrontare questa fase. -
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. -
LEARN FOR FREE What is a KOL? How to approach him? And, most importantly, how can he foster your business? This video course will provide you with insights about the world of KOLs and influencers in the Medtech and healthcare industry. Moreover, you will find out how KOLs can support the medtech development process and drive the success of your startup company! -
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.
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
