Electrical Engineering Expert Witness Blog
Premarket Approval (PMA)
Premarket Approval (PMA) is a cornerstone of the U.S. Food and Drug Administration’s (FDA) strategy to ensure that high-risk medical devices meet stringent standards for safety and effectiveness before reaching the market.
510(k) Clearance
The 510(k) clearance process plays a vital role in medical device regulation, allowing manufacturers to bring new products to market efficiently while ensuring safety and effectiveness.
Medical Device Litigation Expert Witness
Medical device litigation has seen a sharp increase due to the complexity of modern healthcare technology.
Failure Mode and Effects Analysis (FMEA)
Failure Mode and Effects Analysis (FMEA) is a structured methodology for identifying and mitigating potential failures in products, processes, or systems.
Medical Device Development
In the fast-evolving landscape of medical technology, the integration of electrical engineering expertise is critical to ensuring the safety, functionality, and compliance of medical devices.
Crucial Safety Checks: GFCIs and Electrical Engineering Expert Witnesses in Automotive Design
Ground Fault Circuit Interrupters (GFCIs) are a crucial component in electrical safety, primarily used in residential and industrial electrical systems.
Printed Circuit Board (PCB)
Printed Circuit Boards (PCBs) are the foundation of modern electronic devices, providing the necessary interconnections for components to function efficiently.
International Residential Code (IRC)
Understanding the IRC is crucial for builders, contractors, code officials, and even homeowners embarking on construction or renovation projects.
