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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 the Premarket Approval course we will provide regulatory information on the Premarket Approval process. -
The Safer Technology Program Video Course is designed to help you discover STeP and how to navigate program principles and structure. -
The Clinical Laboratory Improvement Amendments Video Course is designed to help you discover the CLIA and how to determine and apply for CLIA waiver or Dual 510(k) by application studies. -
Welcome to the Meditrial training on FDA IVD Regulation. In this training, you will learn what an IVDs are and the factors needed for regulation and classification. -
In this Meditrial Video Course you will learn about critical decision points in the decision-making process FDA uses to determine substantial equivalence. -
In this training, you will learn what IDE means, and how to prepare and submit your application to the FDA. -
LEARN FOR FREE This course will cover some basic concepts to review the reimbursement system and define the role of health economics and outcomes research and will focus on how to incorporate health economics in the market access strategy.
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
