Design for Manufacturability (DfM): Why It Matters and How to Build It In from Day One
Design for Manufacturability shortens time to market, protects margins, and cuts the odds of a late-stage redesign. The catch is sequencing: it only works when manufacturability is evaluated alongside performance and cost, not after tooling is cut. A look at what DfM means in practice for complex device programs.
PiSA USA’s Marie O’Malley to Speak at The Future of Sterilization Workshop at MD&M West 2026
PiSA USA announced that Marie O’Malley, Chief Commercial Officer, will speak at The Future of Sterilization Workshop at MD&M West 2026 in Anaheim, California. The session will explore emerging sterilization technologies, regulatory considerations, and strategic implementation approaches for medical device and pharmaceutical manufacturers, highlighting PiSA USA and Centerpiece’s expertise in advanced sterilization, compliance, and supply chain solutions.