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.
PISA-USA Pharma Injection Molding: What It Is, Key Requirements, and How High-Volume, High-Precision Manufacturing Works
Pharmaceutical injection molding is a high-precision process with zero margin for error. From material selection and cleanroom manufacturing to tooling, validation, and automated quality control, every detail impacts patient safety and regulatory compliance. In this article, PiSA-USA breaks down the fundamentals of pharma injection molding, outlines the critical requirements for regulated production, and explains how high-volume, high-precision manufacturing is achieved at scale—backed by decades of technical expertise and global manufacturing leadership.
Film & Tubing Extrusion in Medical Devices: Balancing Flexibility, Barrier Properties, Strength, and Biocompatibility
Film and tubing extrusion may seem like a small part of a medical device, but it directly impacts performance, safety, and long-term reliability. From IV sets to flexible solution bags, the materials and processes behind extrusion determine how well a device withstands pressure, maintains sterility, and interacts with the human body. At PiSA USA, extrusion is more than just a capability — it’s a core part of our vertically integrated manufacturing ecosystem, allowing us to deliver precise, compliant, and fully traceable components within complete end-to-end device assemblies.
ETO vs. Irradiation, Autoclave, and Emerging Sterilization Methods: Choosing the Right Approach for Your Medical Device
Selecting the right sterilization method is one of the most critical decisions in medical device manufacturing. From ETO to irradiation, autoclave, and emerging modalities like chlorine dioxide and X-ray, each technology offers unique advantages and limitations. This article explores how ethylene oxide (ETO) continues to set the standard for complex and heat-sensitive devices—while comparing it to other leading sterilization methods in terms of compatibility, efficiency, and scalability.
PiSA USA’s Marie O’Malley to Join MassMEDIC Fireside Chat on Technology Challenges in MedTech
PiSA USA is excited to share that Marie O’Malley, Vice President of Commercial Operations, will be a featured speaker at MEDevice Boston 2025. O’Malley will join MassMEDIC’s Fireside Chat: Breaking Barriers — Leading Through Technology Challenges in MedTech on October 1, 2025, bringing nearly 30 years of industry expertise to the stage. Known for her leadership in innovation, supply chain, and regulatory compliance, O’Malley will discuss how collaboration and forward-thinking strategies can turn technology challenges into opportunities for safer, more sustainable solutions.
Mitigating Supply Chain Risk with Nearshore Manufacturing in Mexico
In today’s volatile global market, pharma and medical device companies can’t afford supply chain setbacks. That’s why more organizations are turning to nearshore manufacturing in Mexico—a solution that combines speed, cost efficiency, and regulatory confidence. At PiSA USA, our partnership with Centerpiece in Tijuana takes this a step further, offering end-to-end support from design and clean-room manufacturing to world-class ETO sterilization and compliant warehousing. Together, we’re helping companies cut lead times from weeks to days, reduce risk, and build resilient supply chains ready for tomorrow’s challenges.
Streamlining Development Processes: How PiSA USA Optimizes Efficiency and Reduces Time to Market
In the fast-paced world of medical devices and pharmaceuticals, optimizing development processes is essential to stay ahead of the competition. At PiSA USA, our integrated approach, cross-functional teams, advanced project management, regulatory expertise, state-of-the-art technology, agile methodologies, client-centric collaboration, and commitment to continuous improvement collectively contribute to streamlining development processes
Marie O’Malley Of PiSA USA On How We Can Increase Women’s Engagement in Leadership and Management
Our very own Marie O'Malley has been featured in a Medium article "Marie O’Malley Of PiSA USA On How We Can Increase Women’s Engagement in Leadership and Management." Read the full article here.
Safeguarding Quality: How Automation Enhances Compliance in Medical Device Manufacturing
In the fast-evolving landscape of medical device manufacturing, ensuring compliance with strict regulatory standards is paramount. For large OEM companies seeking contract manufacturing services, the ability of a partner to safeguard quality while maintaining compliance is non-negotiable. In this blog, we examine how automation plays a pivotal role in enhancing compliance within the realm of medical device manufacturing.
Navigating the Complexities of Medical Device Supply Chains - A Call to Action for Manufacturers
From medications and personal protective equipment (PPE) to medical devices and testing kits, hospitals across the nation grapple with acute shortages that pose a threat to patient care and safety. In this dire situation, medical device manufacturers stand at the forefront, holding the key to addressing the crisis and ensuring the resilience of the healthcare system.