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Master of Biomedical Innovation and Development

You are here: Home / Master of Biomedical Innovation and Development (MBID) Program

Master of Biomedical Innovation and Development (MBID) Program

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Professional master’s degree for students seeking a unique specialization in an entrepreneurial, innovative field.


The students of this program are trained on the processes involved in life cycle medical device development to enable global product launches.

How to Apply

Who Should Apply

Ideal candidates for this program include:

  • Aspiring students who wish to pursue a career in Biomedical Product Development such as medical devices.
  • Early-career professionals working in biomedicine.
  • High-performing recent graduates from undergraduate disciplines such as:
  • Engineering, Science, Business & Medicine.

Requirements

  • Classroom and design studio courses will be taught on the Georgia Tech campus in Atlanta.
  • Clinical/experiential courses may be conducted at allied medical institutions and/or selected biomedical industry sites throughout the greater Atlanta area.

MBID Graduation July 25, 2019

Schedule

The MBID master’s program is a one-year residential program that is completed in three sequential semesters over 12 months.  Candidates enroll in the fall semester and take four courses (fall & spring semester) and three courses (summer semester).

Course of Study

The following curriculum presents the 12-month course of study required to earn the MBID professional master’s degree. Learn More

Tuition & Fees

Please visit the Office of the Bursar for the current tuition rate and fees. Learn More

FAQs

Some of the more common general questions about the MBID master’s program. Learn More

Program Brochure

Brochure is available for download in Adobe Acrobat Format. Learn More

Unique Highlights of the Program

The students of this program are trained on the processes involved in life cycle medical device
development to enable global product launches. The training comprises the following functions and domains of expertise.

Pre-Clinical R&D

Comprising the horizon from early concept evaluations and concept prototyping through
pre-clinical development and testing for regulatory
submission.

Regulatory and Clinicals

Covering all aspects of
preparing submissions for global approvals such as 510ks, IDE/PMAs, CE file and country-specific
submissions as well as conducting clinical studies and preparing reports for regulatory submissions.

Quality Assurance

Covering the elements of design controls, change controls, non-conformances, CAPA, etc.

Manufacuturing Scale-Up and Validations

For commercial release in global markets.

Start building your career today!

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Coulter Department of Biomedical Engineering
Emory University
1760 Haygood Drive, Suite W 200
Atlanta, GA 30322
404.727.9874

Georgia Institute of Technology
313 Ferst Drive
Atlanta, GA 30332
404.385.0124
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