• 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.
  • 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.
  • 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!
  • LEARN FOR FREE This Meditrial Video Course explains the fundamental concepts of GDPR and clarifies the impact of this regulation on the conduct of clinical trials.
  • This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR).
  • Is your Clinical Evaluation ready for the MDR? Discover Meditrial e-learning and avoid delays for market access. Meditrial will guide you with easy steps. Learn at your own pace and reach your goals! After the course, you can take a brief test to receive your certification. Enjoy!
  • This lecture describes the key changes in the international ISO standard for clinical trials. In this module we will show you the main changes that have occurred compared to the ISO 14155 2011 in the safety and adverse event reporting.
  • MDR is finally here and takes effect in May 2020! This video lecture provides you with an overview of the new regulations and clinical responsibilities set forth by the new ISO 14155 2020.
  • 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.
  • This tutorial aims to provide an overview of the MDR provisions related to the end of the clinical investigation, along with an outline of the MDR rules concerning the extraordinary events which could happen during the clinical investigation (substantial modifications, corrective measures, temporary halt, early termination).

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