Matt McFarlane

Greenlight Guru

Matt McFarlane is the senior content writer at Greenlight Guru. He’s an avid reader and writer specializing in the medical device industry and its many regulations, standards, and guidance documents.

Wed, 04/02/2025 - 12:02
What Is an MCP Server? And how can medtech companies use one with their QMS?
Thu, 04/30/2026 - 12:02
It can be surprisingly difficult for businesses to get accurate answers to questions about their own data. Often, the data live in different systems or aren’t easily accessible to employees without specific technical skills. Some data may be in…
What FDA Investigators Will Look for Under QMSR How to future-proof your QMS
Wed, 01/21/2026 - 12:01
The medical device industry is counting down to an important deadline: On Feb. 2, 2026, the U.S. Food and Drug Administration’s new Quality Management System Regulation (QMSR) formally replaces the Quality System Regulation (QSR). Although the full…
Facing Medtech Uncertainty How medical device companies are navigating current economic conditions
Thu, 05/29/2025 - 12:02
One of the key findings in Greenlight Guru’s 2025 Medical Device Industry Report was that economic uncertainty is playing a large role in the decisions medical device companies make this year. The report surveyed more than 500 medical device…
2025 Medical Device Industry Report Quality challenges, regulatory complexity, and economic uncertainty
Wed, 04/02/2025 - 12:02
The medical device industry is growing. Data from KPMG predict that global annual sales will rise by 5% per year to reach just under $800 billion by 2030. New technology, new opportunities, and, as always, the promise of improving patient outcomes…