От 2 545,00 $ до 3 190,00 $ This certificate is achieved by completing four (4) core and five (5) elective courses. After successfully completing all nine courses, you will receive a ...

These Regulatory Affairs in the Medical Device Industry aim to protect the patient and ensure health benefits.

This Masterclass will provide you with a comprehensive understanding of the US regulatory procedures for medical devices, to enable you to make recommendations ...

The Regulatory Affairs for Medical Devices certificate provides professionals with the essential knowledge to work in this highly regulated environment and the ...

Medical Device regulatory affairs is a profession developed as a result of the government's concern to safeguard public health by controlling the safety and ...

The FDA's Center for Devices and Radiological Health (CDRH) is responsible for regulating firms who manufacture, repackage, relabel, and/or import medical ...

31 мар. 2024 г. · Regulatory affairs play a pivotal role in the lifecycle of medical devices, guiding products from concept to market while ensuring compliance ...

Our medical device & IVD regulatory experts can help you gain a deep understanding of the applicable regulations and requirements.

This programme will teach students about regulatory rules and principles, in addition to explaining the context in which these rules were developed.

13 мар. 2018 г. · Regulatory affairs professionals serve a critical function throughout a product's lifecycle—particularly in the medical device industry.