Articles by Rebecca Kozodoy

In medical device manufacturing, precision is not optional. Every molded component must meet exacting requirements for safety, reliability, and compliance.

In 2025, medical device manufacturers are grappling with heightened regulatory uncertainty, leading to slower reviews and communication difficulties with the FDA. This situation drives them to reassess operations for compliance and risk management, with a strong emphasis on maintaining product quality, which is vital for patient safety.

Contract manufacturers can enhance their competitive advantage by applying quality best practices from the medical and aerospace industries, both of which demand flawless performance and strict contamination control.