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Clinical Evaluation 2020

Clinical Evaluation Upgrade to MDR
Clinical Evaluation 2020
Summary
Duration:  Unlimited
Cost:  79  USD

Clinical Trials

Clinical Investigation Monitoring - GCP SOPs
Clinical Trials
Summary
Coronary sinus Reducer for the Treatment of refractory angina
Clinical Trials
Summary
Clinical Trial Information System (CTIS)
Clinical Trials
Summary
Duration:  Unlimited
Cost:  99  USD
Good Clinical Practice for Drugs and Medical Devices
Clinical Trials
Summary
Duration:  Unlimited
Cost:  49  USD
Training on Meditrial Good Clinical Practice (GCP) procedures
Clinical Trials
Summary
Clinical Site Selection
Clinical Trials
Summary
Readiness for GCP Audit
Clinical Trials
Summary
Duration:  Unlimited
Cost:  299  USD
Study Approval In EU Countries
Clinical Trials
Summary
Compassionate Use Approval Procedures
Clinical Trials
Summary

Clinical Trials for Medical Devices in Europe

6. MDR ADVERSE EVENT REPORTING IN CLINICAL INVESTIGATIONS
Clinical Trials for Medical Devices in Europe
Summary
Duration:  Unlimited
Cost:  179  USD
5. MDR SUBSTANTIAL STUDY CHANGES, TEMPORARY HALT AND TERMINATION
Clinical Trials for Medical Devices in Europe
Summary
Duration:  Unlimited
Cost:  179  USD
4. MDR STUDY APPLICATION AND APPROVAL - NEW COORDINATED ASSESSMENT
Clinical Trials for Medical Devices in Europe
Summary
Duration:  Unlimited
Cost:  179  USD
3. MDR CONDITIONS, ETHICAL PRINCIPLES, METHODS, INFORMED CONSENT
Clinical Trials for Medical Devices in Europe
Summary
Duration:  Unlimited
Cost:  179  USD
Clinical Trials for Medical Devices in Europe - COMPLETE TRAINING PROGRAM
Clinical Trials for Medical Devices in Europe
Summary
Duration:  Unlimited
Cost:  1074  USD
1. MDR NEW DEFINITIONS AND TYPES OF TRIALS
Clinical Trials for Medical Devices in Europe
Summary
Duration:  Unlimited
Cost:  179  USD
2. MDR THE ACTORS: SPONSOR, INVESTIGATOR & SUBJECT
Clinical Trials for Medical Devices in Europe
Summary
Duration:  Unlimited
Cost:  179  USD

Clinical Trials in US

INVESTIGATIONAL DEVICE EXEMPTION (IDE)
Clinical Trials in US
Summary
Duration:  Unlimited
Cost:  79  USD
HOW TO PREPARE FOR A U.S. MEDICAL DEVICE CLINICAL TRIAL
Clinical Trials in US
Summary
Quality Management System for Medical Devices and Clinical Trials
Clinical Trials in US
Summary
Duration:  Unlimited
Cost:  49  USD

Covid-19

Covid-19 e Sicurezza nel Lavoro - Riascolta il webinar
Covid-19
Summary
Covid-19 e Mental Health - Riascolta il Webinar
Covid-19
Summary
COVID-19 PPE Emergency
Covid-19
Summary
Duration:  Unlimited
Cost:  49  USD
Clinical Trials During COVID-19
Covid-19
Summary
Duration:  Unlimited
Cost:  49  USD

Digital Health

Digital Health: What is it? Why Does it Matter?
Digital Health
Summary
Digital Health Revolution
Digital Health
Summary
The Virality Of Digital Health
Digital Health
Summary

Europe Market Access

Southern Europe Market Access
Europe Market Access
Summary
Duration:  Unlimited
Cost:  49  USD
Eastern Europe Market Access
Europe Market Access
Summary
Duration:  Unlimited
Cost:  49  USD
Western Europe Market Access
Europe Market Access
Summary
Duration:  Unlimited
Cost:  49  USD
Northern Europe Market Access
Europe Market Access
Summary
Duration:  Unlimited
Cost:  49  USD

FDA Medical Device Regulation for Everyone

HOW TO FIND AND EFFECTIVELY USE PREDICATE DEVICES
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
FDA IVD REGULATION
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
FDA EARLY FEASIBILITY STUDY PROGRAM
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
510(k) Submission Process
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  69  USD
FDA Q-Submission Process
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  89  USD
Breakthrough Device Designation
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
Emergency Use Authorization (EUA)
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
De Novo Classification Pathway
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
FDA Clinical Laboratory Improvement Amendments (CLIA)
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
FDA Safer technology program (STeP)
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
FDA Premarket Approval (PMA)
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  79  USD
FDA Medical Device Development Tools (MDDT) Program
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD
Monitoring for Medical Devices in the US Essential FDA Guidelines
FDA Medical Device Regulation for Everyone
Summary
Duration:  Unlimited
Cost:  49  USD

GDPR

GDPR & Clinical Trials
GDPR
Summary
GDPR Compliance
GDPR
Summary
Duration:  Unlimited
Cost:  49  USD

ISO 14155:2020 GCP for Medical Devices

INNOVATIONS IN GLOBAL CLINICAL TRIALS
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  99  USD
ISO 14155 2020 Safety and Adverse Events
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  99  USD
New ISO 14155 2020 Key Changes for your Trial
ISO 14155:2020 GCP for Medical Devices
Summary
ISO 14155 2020 Overview
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  49  USD
ISO 14155 2020 New Responsibilities of Sponsor/CRO
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  99  USD
ISO 14155 2020 Responsibilities of Principal Investigator
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  99  USD
ISO 14155 2020 Masterclass
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  495  USD
ISO 14155 2020 Ethical Considerations
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  99  USD
ISO 14155 2020 Clinical Trial From Start To Finish
ISO 14155:2020 GCP for Medical Devices
Summary
Duration:  Unlimited
Cost:  99  USD

Medical Device Clinical Trials in Germany - MPG CME Certified Courses

MDR/MPDG Update Course - Online
Medical Device Clinical Trials in Germany - MPG CME Certified Courses
Summary
Duration:  Unlimited
Cost:  350  EUR
MPG Auffrischungskurs - Onlinekurs
Medical Device Clinical Trials in Germany - MPG CME Certified Courses
Summary
Duration:  Unlimited
Cost:  400  EUR
MPG Grundlagenkurs - Onlinekurs
Medical Device Clinical Trials in Germany - MPG CME Certified Courses
Summary
Duration:  Unlimited
Cost:  500  EUR

Medical Device Revolution

10. Privacy, GDPR e Medical Device
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
9. ITALIA: Normative e Procedure di approvazione, gestione centri, monitoraggio e report di sicurezza
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
8. Digital Health, eCRF/ePRO, Data Management, Cybersecurity
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
7. ISO 14155: il monitoraggio per i Medical Device in pratica
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
6. ISO 14155 Conduzione dello studio dalla A alla Z
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
5. ISO 14155 Fondamenti, Disegno e pianificazione dello studio, la documentazione
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
4. EUROPA i Trial Clinici, le nuove regole, cosa cambia e come prepararsi
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
3. EUROPA Nuovo Regolamento: panoramica e punti critici per le CRO
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
2. Orizzonti del Medical Device, Regolamenti Globali, Roadmap to Market
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD
1. Il mondo del medtech, biotech e digital health - capire la classificazione e il mercato
Medical Device Revolution
Summary
Duration:  Unlimited
Cost:  99  USD

New In Vitro Device Regulation (IVDR)

In Vitro Medical Device Regulation Roadmap (IVDR)
New In Vitro Device Regulation (IVDR)
Summary
Duration:  Unlimited
Cost:  49  USD
IVDR ISO 20916:2019
New In Vitro Device Regulation (IVDR)
Summary
Duration:  Unlimited
Cost:  49  USD
European IVDR Masterclass
New In Vitro Device Regulation (IVDR)
Summary
Duration:  Unlimited
Cost:  79  USD

New Medical Device Regulation (MDR)

Medical Device Day
New Medical Device Regulation (MDR)
Summary
HEOR CRASH COURSE REAL WORLD
New Medical Device Regulation (MDR)
Summary
MDR ROADMAP FOR YOUR CLINICAL TRIALS
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  179  USD
MDR Requirements for device labeling and implant card
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
MDR The New European UDI System (Part 2)
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
MDR The New European UDI System (Part 1)
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
INTRODUCTION TO MEDICAL DEVICE REGULATION ROADMAP & ORIENTATION
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
INNOVAZIONE NEL MONDO DELLA RICERCA CLINICA
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
MDR EUDAMED The European Database for Medical Devices and IVDS 
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
MDR FOR DUMMIES
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
Post-Market Clinical Follow-Up
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
Post-Market Surveillance for Medical Devices in Europe
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  49  USD
Medical Device Regulation Roadmap And Orientation
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  79  USD
MDR Fundamentals
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  79  USD
New Medical Device Regulation (MDR) Master Class
New Medical Device Regulation (MDR)
Summary
Duration:  Unlimited
Cost:  989  USD

Pharmacovigilance

EUDRAVIGILANCE CERTIFIED TRAINING
Pharmacovigilance
Summary
The Pharmacovigilance System in Europe - Chinese
Pharmacovigilance
Summary
European Pharmacovigilance and Drug Safety Training
Pharmacovigilance
Summary

Product Guidelines and Standards

Lesson 3 - Design and Conduct Clinical Trials for Transcatheter Occluders ISO 22679
Product Guidelines and Standards
Summary
Duration:  Unlimited
Cost:  99  USD
Lesson 2 - Device Design, Pre-Clinical Testing and Risk MGT
Product Guidelines and Standards
Summary
Duration:  Unlimited
Cost:  99  USD
Lesson 1 - Introduction to ISO 22679
Product Guidelines and Standards
Summary
Duration:  Unlimited
Cost:  99  USD
PayPal
Transcatheter Cardiac Occluders - ISO 22679 - Complete course
Product Guidelines and Standards
Summary
Duration:  Unlimited
Cost:  282.15  USD

Startup and Business Practices

Fastrack to Success: How to Build a Regulatory and Clinical Strategy
Startup and Business Practices
Summary
Startup Governance: A 10-Step Guide for innovators and board members
Startup and Business Practices
Summary
Duration:  Unlimited
Cost:  149  USD
Win KOLs and work with Partners
Startup and Business Practices
Summary
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