Articles By Eric Larson
-
10.08.25 -- FAQs On The Revised EU GMP Annex 1
10/8/2025
10/08/25 Med Device Online Newsletter
-
The No-BS Guide To MES For Medical Device Manufacturers
10/7/2025
Legacy MES systems slow NPIs and complicate audits. Learn how a composable MES enforces SOPs, integrates BOMs, and speeds up onboarding with digital workflows, e-signatures, and real-time tracking.
-
Smith+Nephew's Agile Digital Transformation In Med Device Manufacturing
10/7/2025
Explore how real-time insights, targeted digital tools, and agile workforce strategies can elevate quality, streamline compliance, and accelerate ROI without relying on outdated software models.
-
10.07.25 -- Companion Diagnostic Strategy For Combination Product Success
10/7/2025
10/07/25 Med Device Online Newsletter
-
Key Considerations For Selecting A Solenoid Valve In Health & Science Applications
10/7/2025
Solenoid valves are vital in medical devices, enabling precise fluid and gas control. Explore customizable, high-reliability valves that optimize performance while conserving space, weight, and power.
-
10.05.25 -- RFK Jr. Wants Every American Wearing A Wearable. How Can Pharma Build A Business Around It?
10/5/2025
10/05/25 Med Device Online Newsletter
-
10.04.25 -- September's Most Popular Articles & Solutions
10/4/2025
10/04/25 Med Device Online Newsletter
-
The Balkan Puzzle: Using Non-EU States As A "Pre-MDR" Proving Ground For Your Device
10/3/2025
The EU's Medical Devices Regulation (MDR) has introduced a new level of rigor. A sophisticated, yet practical, strategy is emerging: leveraging non-EU Balkan countries as a "pre-MDR" proving ground.
-
Trust But Verify: Validating AI In Pharma's GxP World
10/3/2025
Here are practical tips to build validated, transparent, and auditable AI systems that align with GxP principles, paving the way for smarter and more resilient manufacturing processes.
-
Biocompatibility Studies: Prepare For Change
10/2/2025
Stay ahead of evolving regulations by learning the latest updates, testing strategies, and expert guidance to strengthen the safety and compliance of your medical devices.