Training tutorial
Courses tagged with "Training tutorial"
Quality Management System for Medical Devices and Clinical Trials
Clinical Trials in USThis 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.
COVID-19 PPE Emergency
Covid-19Time: 15 Minutes
Clinical Trials During COVID-19
Covid-19Video Course
Time: 22 Minutes
FDA Q-Submission Process
FDA Medical Device Regulation for Everyone
Breakthrough Device Designation
FDA Medical Device Regulation for Everyone
Emergency Use Authorization (EUA)
FDA Medical Device Regulation for Everyone
De Novo Classification Pathway
FDA Medical Device Regulation for Everyone
FDA Medical Device Development Tools (MDDT) Program
FDA Medical Device Regulation for Everyone
Monitoring for Medical Devices in the US Essential FDA Guidelines
FDA Medical Device Regulation for Everyone
What is GDPR?
When is it applicable?
Fines for Non-Compliance
GDPR and Clinical Trials
How to comply, practical approach
LEARN FOR FREE
RECORDED LIVE LECTURE - Dr. M. Tocchi
Time: 15 Minutes
This recorded video-lecture by Dr. Monica Tocchi, who contributed to the development of international standard ISO 14155 for clinical trials. This introductory course describes the key changes that affect pre-market studies and post-market trials for medical devices.
European IVDR Masterclass
New In Vitro Device Regulation (IVDR)
INTRODUCTION TO MEDICAL DEVICE REGULATION ROADMAP & ORIENTATION
New Medical Device Regulation (MDR)This course presents an overview of the new European regulation for medical devices and provides key information regarding new changes within the MDR. Learn all you need to know for a successful transition to the new legislative framework.
After the course, you can take a brief test to receive your certification. Enjoy!
MDR EUDAMED The European Database for Medical Devices and IVDS
New Medical Device Regulation (MDR)This video course presents the European Database for Medical Device and in vitro diagnostic device and provides key information in order to become familiar with the new electronic system for data storage. Learn all you need to know regarding the new Electronic database system.
Post-Market Clinical Follow-Up
New Medical Device Regulation (MDR)This lecture describes the key changes regarding post market clinical follow-up and what companies should do to meet their new obligations. After the course you can take a final test to receive your certification. Enjoy!
Post-Market Surveillance for Medical Devices in Europe
New Medical Device Regulation (MDR)Video Course
Time: 25 Minutes
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!
The Pharmacovigilance System in Europe - Chinese
PharmacovigilanceIn response to the global need for training in pharmacovigilance and the regulation changes in Europe, Meditrial has developed a series of e-learning courses covering different aspects of the science of medicines safety.
Meditrial’s e-learning courses take a micro-learning approach, with short, concise lessons connected to clear learning objectives. Most courses are taught in English, with subtitles in English. Courses are also available in other languages such as German, Italian and Chinese. Upon completing a course, you will take a final test to receive a digital certificate that can be printed.
The broad collection of self-paced e-learning courses is suitable to health professionals with an interest in pharmacovigilance. Courses are made available free of charge to those working at pharmacovigilance centres or in the public sector (hospitals, pharmacies, academia etc.). For those working at for-profit organisations or companies (pharmaceutical companies, contract research organisations etc.), the courses will be made available for a fee. Please visit our e-learning platform to enrol and learn more about the course content.
European Pharmacovigilance and Drug Safety Training
PharmacovigilanceIn response to the global need for training in pharmacovigilance and the regulation changes in Europe, Meditrial has developed a series of e-learning courses covering different aspects of the science of medicines safety.
Meditrial’s e-learning courses take a micro-learning approach, with short, concise lessons connected to clear learning objectives. Most courses are taught in English, with subtitles in English. Courses are also available in other languages such as German, Italian and Chinese. Upon completing a course, you will take a final test to receive a digital certificate that can be printed.
The broad collection of self-paced e-learning courses is suitable to health professionals with an interest in pharmacovigilance. Courses are made available free of charge to those working at pharmacovigilance centres or in the public sector (hospitals, pharmacies, academia etc.). For those working at for-profit organisations or companies (pharmaceutical companies, contract research organisations etc.), the courses will be made available for a fee. Please visit our e-learning platform to enrol and learn more about the course content.
This course includes selected guides of Catchtrial eTMF and ISF training program, for MOCA I CorFlow.
By reading the course documentation, the User will be able to access and review eTMF documents stored in Egnyte and understand the structure of the ISF.
At the end of the course, a quiz made of #5 questions is available. Upon successfully answering at least #4 of the #5 questions, the User will get the training certificate.
Welcome to CorFlow MOCA I - eCRF Training for CRA, a guide for training study Monitors on Catchtrial EDC features implemented for MOCA I data capture and images transfer.
By reading the course documentation, the Monitor will be able to access and review the eCRF data, manage system queries (manual an automated), perform electronic Source Data Verification, lock the verified clinical data.
This course includes a final quiz made of #5 questions. Upon successfully answering at least #4 of the #5 questions, the Monitor will get the training certificate.
