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How to run a startup successfully? The success of your business depends on the mix of innovative ideas and skilled board members. This video course will offer you a 10-Step Guide to quickly understand what you need to do to accomplish your goals and achieve the business targets for your MedTech company. -
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This course will help you to discover new definitions and types of trials as well as the main actors involved, specifically sponsor, investigator and subject. You will also learn about conditions, ethical principles, methods and the informed consent process and develop a better understanding of the new coordinated assessment. You will also gain key knowledge regarding substantial changes, temporary halt, and termination as well as adverse event reporting. -
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This course will help you develop a broader understanding of the new standard, ethical considerations and how to conduct a clinical trial from start to finish. You will also discover the new responsibilities of sponsor/CRO and principle investigator, and learn about safety and adverse events under the new standard. -
In this course you will get an overview of worldwide pharmacovigilance standards. Here we also talk about the main goals of pharmacovigilance in clinical research. In addition, we will shed the light on various ways how one can ensure the safest use of a drug and its compliance with the legal requirements on pharmacovigilance. Upon completing a course, you will take a final test to receive a digital certificate that can be printed. -
In this course you will learn about all the MDR rules on medical device labelling, dwelling on the language, label content requirements, and updates according to data of the Post-market surveillance system. -
The second part of New European UDI System Video Course is designed to help you discover UDI Implementation, Medical Device Registration, and functional specifications. This course also covers the data dictionary for UDI as well as the MDCG guidelines on UDI-DI and for special cases of device registration. -
LEARN FOR FREE 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. -
This Meditrial Video Course is designed to help you discover the FDA De Novo Classification Pathway and intended to provide De Novo requesters with transparency regarding the process of submission De Novo Classification request. -
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! -
In this Meditrial Video Course you will learn about critical decision points in the decision-making process FDA uses to determine substantial equivalence.
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
