Webinar Replay

Courses tagged with "Webinar Replay"

Scientific Discussion on the treatment of refractory angina. 

Dr. Konigstein presents the results of the latest publication on a novel treatment for this challenging clinical problem.

Category: Clinical Trials
Length: 00:40

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This exclusive educational event is reserved to selected Meditrial customers and Meditrial’s staff. With COVID 19, medical device companies are facing increasing complexity to conduct their clinical trials in the US.

Length: 01:00
Duration:  Unlimited
Cost:  49  USD

This recorded lecture, given by Charisse Green, Global Quality Expert, will help you discover the fundamental concepts of global quality for medical devices and clinical trials. She brings to you her professional perspective which stems from her extensive background as an FDA inspector.

Length: 00:20
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Parliamo di nuovo del problema delle mascherine, che diventa fondamentale nella fase di ripartenza dopo l’emergenza covid.
Non siamo qui per ripetere quanto già diffuso dalla stampa e su internet, ma focalizzarci su quello che dovrebbe sapere sia chi compra, sia chi produce, soprattutto le aziende riconvertite.
Category: Covid-19
Length: 01:00
Version: 01
Release Date: 9 June 2020

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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.

Category: Covid-19
Length: 01:00
Version: 01
Release Date: 2 June 2020

FDA Medical Device Development Tools (MDDT) Program

FDA Medical Device Regulation for Everyone
Duration:  Unlimited
Cost:  49  USD
This recorded lecture, given by Charisse Green, Global Quality Expert, will help you discover the Medical Device Development Tools Program, this program is a way for the FDA to qualify tools that medical device sponsors can use in the development and evaluation of medical devices.
Length: 00:20
Duration:  Unlimited
Cost:  49  USD
This recorded lecture, given by Charisse Green, Global Quality Expert, will help you discover the monitoring essential guidelines for medical devices in the US. She brings to you her professional perspective which stems from her extensive background as an FDA inspector.
Length: 00:10

INNOVATIONS IN GLOBAL CLINICAL TRIALS

ISO 14155:2020 GCP for Medical Devices
Duration:  Unlimited
Cost:  99  USD
WEBINAR REPLAY 
This webinar provides an overview of the innovations in clinical trials and provides practical suggestions on how to get ready now – as the standard is already effective and everyone is expected to comply!
Length: 00:30

Medical Device Day

New Medical Device Regulation (MDR)
Viaggio nel mondo delle Tecnologie Medicali e Digital Health.
L’Università degli Studi di Roma Tre e Meditrial presentano una giornata dedicata al mondo dei Medical Device all’interno del Master Sociosanitario. Le testimonianze di esperti, protagonisti nel settore sanitario, socio-sanitario e socio-educativo, racconteranno l’evoluzione del panorama globale in ambito MDR a livello clinico e regolatorio.
Length: 06:00

MDR ROADMAP FOR YOUR CLINICAL TRIALS

New Medical Device Regulation (MDR)
Duration:  Unlimited
Cost:  179  USD

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.

"Meditrial has been preparing for the MDR for 3 years. Alignment with our customers is key to our joint success. We believe that sharing our learnings with you will facilitate understanding and handling the changes together. With this course, we wish to provide you practical information and answers for your MDR compliance."
Dr. Monica Tocchi
Length: 01:30

INNOVAZIONE NEL MONDO DELLA RICERCA CLINICA

New Medical Device Regulation (MDR)
Duration:  Unlimited
Cost:  49  USD
Il mondo della ricerca clinica sui Medical Device sta subendo in questi anni una forte evoluzione dovuta all'incremento degli standard di qualità che in tempi brevissimi dovranno raggiungere il livello delle sperimentazioni con farmaco. Per questo motivo è fondamentale per chi lavora in questo ambito, ma anche per chi vuole ampliare le proprie prospettive, conoscere quali saranno gli scenari futuri dovuti a questa rivoluzione.

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.

Win KOLs and work with Partners

Startup and Business Practices
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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 success of your company!

Length: 00:45
Version: 01
Release Date: 3 June 2020