Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
July 9, 2024Journal of Engineering Research and ReportsOpen Access

Methods for Medical Device Design, Regulatory Compliance and Risk Management

View Full Paper
Ask AI
Bookmark
Share

Authors

JSJagbir SinghPPPriyank Patel

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Singh et al. (2024) studied this question.

synapsesocial.com/papers/68e60e4db6db6435875a145chttps://doi.org/10.9734/jerr/2024/v26i71216
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Review of Medical Device Design2024 · 1 citations
  2. 2Regulatory Issues Encountered in the Process of Medical Device Project Management2024 · 2 citations
  3. 3The Critical Role and Practice of Medical Device Design and Development Documentation in Quality Systems2025 · 1 citations
  4. 4Synergizing Design for Manufacturability (DfM) and Quality by Design (QbD) to Optimize Product Development in Medical Device Manufacturing2025
  5. 5Methodologies for mapping existent common specification, standards, and overlapping regulation for medical devices: a scoping review2026 · 1 citations