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Discover the world of innovation and medical standards made easy, learn about the brand new ISO 22679 draft standard for cardiac occluders. -
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. -
Get Certified Today!
Do you need an MPG certificate to carry out clinical trials with medical devices? Would you like to deepen your knowledge? This Mastertrial MPG/GCP course is all online and is recognized by the Berlin Medical Association (CME). This Refresher Course offers the following accredited training course for principal examiners, examiners and members of the examination group. Download the MPG courses brochure -
Get Certified Today!
Do you need an MPG certificate to carry out clinical trials with medical devices? Would you like to deepen your knowledge? This Mastertrial MPG/GCP course is all online and is recognized by the Berlin Medical Association (CME). This Basic Course offers the following accredited training course for principal examiners, examiners and members of the examination group. Download the MPG courses brochure -
Compliance with the new general data protection regulation (GDPR): the present course explains about EU General Data Protection Regulation (GDPR) issued by the European Parliament and the Council of the EU to strengthen and unify data protection for all individuals within the EU. The processing of personal data related to EU subjects for the purpose of clinical trials falls within the scope of the GDPR. -
This video lecture discusses the impact of COVID-19 on clinical trials, potential pathways and modifications needed to run a successful trial and how new technologies can assist in moving forward. -
Sale!
Discover the world of innovation and medical standards made easy, learn about the brand new ISO 22679 draft standard for cardiac occluders. -
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). -
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!
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
