10 Bookmark-Worthy Resources for Medical Device Professionals

Don't you hate it when you scroll upon an article online that looks really useful, but then you can't find it when you need it most? We hate it too. That's why we've compiled this list of MD+DI articles for professionals in the medical device industry to bookmark for future reference on product development, manufacturing, and regulatory topics.

Expected Medical Device Lifetime at a Glance

A distinguished Medtronic engineer shares his knowledge about regulations regarding medical device lifetime expectancy.

De-Risk Your Medical Device Project with Targeted Prototypes and Mock-Ups

Effective prototyping can significantly reduce time to market and overall development cost.

Designing Medical Devices for Manufacturability: How to Do It and Why You Should

Practical advice from three medical device industry experts on how to keep manufacturability top of mind in the design process.

Is 3D Printing Right for Your Medical Device Project?

3D printing is on track to expand beyond prototyping toward end-use parts and mass production, but the economics still don't make sense for every project.

Medtech Incubators and Accelerators: Where Are the Hubs for Medical Device Innovation?

A comprehensive guide to U.S.-based incubators and accelerators serving the medical device industry.

Medical Device Sterilization: 4 Alternatives to Using Ethylene Oxide

Why ethylene oxide is used to sterilize medical devices, plus four alternative sterilization methods to consider.

The Future of Gamma Irradiation for Medical Device Sterilization

Everything you need to know about the role that gamma irradiation plays in medical device sterilization.

Medical Device Design: 3 Practical Tips for Great User Interface and User Experience

Experts at Kablooe Design share practical tips for doing great user interface and user experience (UX/UI) in medical device design.

Understanding Regulatory Expectations for Combination Products

Experts at WuXi AppTec Medical Device Testing answer a few questions about submitting combination products for regulatory approval.

UKCA Compliance: What You Need to Know and Implement by June 2023

Stay up to date on these regulatory developments to continue to market medical devices in the United Kingdom.