Mike on Medtech

Measuring Regulatory/Quality Team Member Performance—Mike on Medtech

Mike Drues and Sean Fenske share ideas and best practices for measuring performance, and also how much to trust these company members.

People

Mike Panos Joins Insulet as Chief Commercial Officer

New hire has 30 years of commercial leadership experience in the medtech sector.

Medtech Makers

Ensuring Scalability Throughout the Medical Device Lifecycle—A Medtech Makers Q&A

During the development of a medical product, the proper steps need to be taken so scaling can take place as needed to meet demand.

Online Exclusives

Partnering for Performance: A New Playbook for Medical Device Manufacturers

Many hospitals are investing in advancing their patient care capabilities and need medtech companies to help them.

Online Exclusives

Stop Running Medtech ‘War Rooms’: Stay Inspection-Ready Every Day

We have to rectify the “War Room” scramble that medtech teams all too often face to assemble records before an audit.

VideoBites

Examining Cross-Border M&A Deals in Medtech—An MPO Videobites

With the global environment for medical device manufacturing, cross-border deals are common and may provide for a unique definition for success.

Online Exclusives

2026 Medical Device Industry M&A Roundup (Updated 5/26)

MPO's catalogue of the medtech market's M&A transactions, updated throughout the year.

VideoBites

The Medtech Industry’s Shift from CMO to CDMO—An MPO Videobites

More and more, medical device OEMs are enlisting the assistance of contract development and manufacturing organizations (CDMOs).

Medtech Makers

The Changing Landscape of Cleaning Validation—A Medtech Makers Q&A

Ensuring a cleaning validation is compliant with the regulatory rules of a particular area or region can be critical to a timely launch in the market.

Medtech Makers

Ensuring Global Quality and Regulatory Compliance—A Medtech Makers Q&A

With differing guidelines and regulations around the globe, staying current on all regions in which a company operates can be challenging.

Mike on Medtech

FDA’s Third-Party Review Program—Mike on Medtech

Mike Drues and Sean Fenske discuss the agency’s program, how it’s used, and why no one really knows much about it.

Medtech Makers

Leveraging DFM to Gain Production Benefits—A Medtech Makers Q&A

Design for manufacturability incorporated early in the development phase can help provide a smooth transition into the manufacturing environment.

People

Augusta University, Georgia Tech Team Up to Boost Medtech Innovation

Augusta University is home to a wealth of researchers in the biomedical and related fields.

Features

Renewed Relationships for Full-Service Medtech Outsourcing

Challenges in recent years have led medical device manufacturers to revisit their outsourcing strategies and engagement with strategic partners.

Datawatch

SaMD: From Side Project to Central Strategy

For medtech’s capital equipment-savvy audience, SaMD is no longer just a digital adjunct.