Medical Device Regulatory Affairs

Institute of Technology Carlow - Carlow Campus

 

Course Name Medical Device Regulatory Affairs
Course Provider Institute of Technology Carlow - Carlow Campus
Course Code CWL34 CWL13 CWL14
Course Type Postgraduate
Qualifications
Award NameNFQ ClassificationAwarding BodyNFQ Level
Degree - Masters (Level 9 NFQ)  More info... Major Institute of Technology Carlow Level 9 NFQ
Postgraduate Diploma (Level 9 NFQ)  More info... Major Institute of Technology Carlow Level 9 NFQ
Apply To PAC
Attendance Options Full time, Part time, Daytime
Location (Districts) Carlow Town
Qualification Letters MSc
PAC Application Information

Expand+Course Codes:
CWL34 Master of Science in Medical Device Regulatory Affairs CARLOW Full-time
CWL13 Master of Science in Medical Device Regulatory Affairs CARLOW Part-time
CWL14 Postgraduate Diploma Medical Device Regulatory Affairs CARLOW Part-time...

Application Weblink Web Page - Click Here
Duration 1 year full-time, 2 years part-time.
Course Fee CWL34 Master of Science in Medical Device Regulatory Affairs CARLOW Full-time 9 60 €5,500**

CWL13 Master of Science in Medical Device Regulatory Affairs CARLOW Part-time €7,400*

CWL14 Postgraduate Diploma Medical Device Regulatory Affairs CARLOW Part-time €5,500

*Fees for ITC Major Award graduates only – €5,500.
** SUSI Funding not available.
Entry Requirements Applicants require a second class honours degree or higher, or an equivalent in a science, business or management subject. Other applicants will be considered on an individual basis in accordance with the Institute policy on Recognition of Prior Learning (RPL). IT Carlow reserves the right to require applicants to attend for an interview to determine their suitability for the programme.
Course Content What is the programme about?
This programme presents a broad view of the regulatory affairs role and provides a detailed insight into current and proposed EU legislation. It provides students with an advanced theoretical understanding of the processes and practices central to medical device regulatory affairs.
Subjects Taught What subjects will I study?

Regulatory Affairs Quality Management and Strategy

Research Methods and Technical Report Writing

Medical Device Technologies: Design, Development and Testing

Medical Technology Regulatory Affairs

Product Programme Management, Vigilance, Surveillance and Risk Management

Clinical Evaluation of Medical Device Technologies

NOTE: Specific modules may be subject to amendment after our 2021 programmatic review.
Number of Credits Master of Science in Medical Device Regulatory Affairs 90 Credits
Postgraduate Diploma Medical Device Regulatory Affairs 60 Credits
Careers or Further Progression

Expand+What will I be able to do when I finish this programme?
This MSc will allow students to develop a set of transferable skills that will directly meet the requirements of future employers including information technology, written and verbal communica...

Further Enquiries LIFELONG LEARNING MANAGER
Eoin O’Brien
BA, DBS, CBS, Cert Mgmt, MBA
E: eoin.obrien@itcarlow.ie