To understand the process of approval for medical devices in different countries
To analyze the applicable standards and regulations for medical device approval
To investigate the role of Information Technology in project lifecycle management in the medical industry
Research and compare the approval process for medical devices in at least three different countries
Analyze the standards and regulations such as FDA in the US and CE Marking in Europe for medical device approval
Explore the use of Information Technology tools such as project management software and data analytics in managing the lifecycle of medical device projects.
