Medical Device Regulatory Affairs Online Course

Medical devices is achieved by completing four core and five elective courses.

Medical device regulatory affairs online course.

The regulatory affairs certificate. After successfully completing all nine courses you will receive a certificate recognizing your achievement. Nonclinical biomedical product regulation study the regulations applicable to biomedical product commercialization from pre clinical development quality and. 22 2020 nov.

Medical device regulatory affairs learn how to apply statutes of the submission of marketing approval applications for medical device products to global regulatory agencies. Medical device courses from top universities and industry leaders. This course is also found in the global medical device regulatory affairs professional certification program. The course is primarily geared towards those who are new to industry or require a basic understanding of medical device regulatory compliance issues.

Online courses for industry on safety and effectiveness of medical devices and exposure to radiation from medical devices. Orau free online courses for state local and tribal regulatory partners. These general studies pathways include four core courses that are required and five electives. This global medical device regulatory affairs professional certification program is an online program which guides the student through a global medical device regulations overview.

First explore the certificate program that suits you best. This online medical device compliance training course has been developed for those who are involved with ensuring regulatory compliance for medical devices. We have dynamic course owners around the world allowing delivery of training in many local languages. Transdisciplinary education for critical hacks of medical devices.

Medical devices are globally regulated by a series of regulations and rules designed to produce an effective and safe device. No one knows better than you what your regulatory learning needs are so who better to build a certificate program that meets them. Design and develop medical devices to international quality standards ensure smooth submission meet iso 13485 standards satisfy customers and keep ahead of all regulatory developments with our medical devices training courses. It discusses how iso13485 2003 the iso standard relates to the industry of medical devices details the regulatory ex.

Online training in regulatory affairs for medical devices. This online course guides you through an overview of regulations that apply to global medical devices.