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Massachusetts Institute of Technology

A study of the challenges faced by FDA-regulated early-stage medical device startups and how to approach them

Abstract

dc:description.abstract

It is never easy to start a company with a novel product, let alone building hardware that will be rigorously regulated by the United States Food and Drug Administrations (FDA). This thesis explores the difficulties faced by startups and proposes a step-by-step guide for the founders to navigate this challenge. The guide seeks information from the regulations database, and from interviews with stakeholders involved in medical product developments. First, the device requirements by the FDA and the device application process are presented in the style of a submission guide. The different costs to the startups are then discussed followed by guidelines to founders to steer their startup ship. The guideline focuses on 1) explaining the personas and challenges faced by the stakeholders in medical device development, 2) presenting the best practices in medical product development, 3) recommendations to adopt an electronic Quality Management System with software and tools and finally 4) pointers to useful resources those founders may have to spend months to collate. This thesis is a starting point for anyone thinking of creating medical devices regulated by the FDA, regardless of background and experience.

Degree

thesis:*
Name thesis:degree_name
Master
Department dc:contributor.department
Massachusetts Institute of Technology. Integrated Design and Management Program
Grantor dc:publisher
Massachusetts Institute of Technology
Year dc:date.issued
2020

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Bui, Chinh (Chinh Thi Diem)
Advisor dc:contributor.advisor
  • Matthew Kressy.

Subjects

dc:subject × 3

Rights

dc:rights
Statement dc:rights
  • MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
Handle dc:identifier.uri
https://hdl.handle.net/1721.1/132807
OAI identifier oai:identifier
oai:dspace.mit.edu:1721.1/132807

Chain of custody

source
Harvested from
MIT
Base URL
dspace.mit.edu/oai/request
Last updated
2026-07-22
Source record
OAI-PMH GetRecord
citation

Bui, Chinh (Chinh Thi Diem). A study of the challenges faced by FDA-regulated early-stage medical device startups and how to approach them. Massachusetts Institute of Technology, 2020. https://hdl.handle.net/1721.1/132807