When creating efficient and cost-effective products, we excel in DFMA. We meticulously analyze how each part and assembly can meet their requirements while ensuring seamless integration. Our goal is to eliminate errors and guarantee flawless assembly every single time.

In the realm of medical device manufacturing, precision, and quality are of utmost importance. Our team is well-versed in design verification and process validation. We rigorously test and validate your products to ensure they meet all design requirements, even accounting for normal input variability. With our expertise in installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ), you can trust that your medical products are in safe hands. We employ comprehensive statistical analysis to validate the operation and performance of your products.

Reliability is a key factor in any design, process, or system. Our engineers employ a systematic approach using Failure Mode Effects Analysis (FMEA) to identify potential risks and determine effective mitigation strategies. Whether it's evaluating the reliability of a design (dFMEA), process (pFMEA), or system (sFMEA), we ensure a thorough assessment throughout the entire lifecycle. By following a formalized and documented FMEA process, we guide your design from inception to a reliable, risk-mitigated solution.