Newsletter | August 14, 2025

08.14.25 -- Minimizing The Impact Of Human Errors Using Relational Risk Analysis

FEATURED EDITORIAL

Minimizing The Impact Of Human Errors Using Relational Risk Analysis

This article describes how a mechanism-based risk analysis approach can provide two complementary opportunities for minimizing the likelihood of a human error impacting pharmaceutical and medical device risks.

INDUSTRY INSIGHTS

What Kind Of Capacitors Does Knowles Make?

Discover capacitors for everything from medical implants to fusion experiments, covering energy storage from millijoules to kilojoules with tailored, high-performance solutions.

What Is A Bowie-Dick Test And Why Is It Important?

Effective sterilization is vital in manufacturing. Discover how the Bowie-Dick test ensures vacuum sterilizer performance, safeguards patient safety, and strengthens your sterility assurance program.

The Benefits Of Partnering Early With An Expert Textile Supplier

Ideally, device engineers should partner with a textile component supplier as soon as possible during the earliest stages of product development. But how can a device manufacturer find the right textile partner?

Choosing PTFE Tubing: Film-Cast vs. Ram-Extruded

With decades of experience in PTFE, explore how a company has mastered extrusion and film-cast techniques and continues to innovate to expand solutions for medical devices.

RESOURCES

Analytical Testing

Ulteeva Purity: Your Vision. Our Fiber.

ARTICLES YOU MAY HAVE MISSED

Medical Device Innovation In Brazil: Success Stories And Future Opportunities

Audit Trail Compliance And What To Look For In Mitigation Software

Navigating FDA Regulatory Changes: Policy Shifts, Deregulation, Restructuring, And Future Oversight

Critical Considerations For IP & Patents For Emerging Medical Device Companies

Cybersecurity Risk Management In Medical Devices: Practical Implementation Of FDA's 2025 Final Guidance

BULLETIN BOARD

Expert Tool Transfer: Ensuring A Rapid Return To Production

Medbio's tool transfer process ensures seamless relocation of medical device manufacturing by assessing tools, implementing improvements, and rapidly resuming production to maintain quality and efficiency.

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