NPG is the leading authority in packaging engineering, driving regulatory compliance, efficiency, and quality, ensuring seamless pathways for products to market.
As the world leader in packaging engineering consulting, NPG stands apart through its deep life sciences expertise and adaptive, partnership-focused model. Our specialized services offer unmatched regulatory insight, flexibility, and comprehensive validation support. NPG delivers tailored, compliant solutions that ensure quality and efficiency, setting industry benchmarks in packaging engineering excellence.
We accelerate product readiness with NPG’s packaging expertise ensuring secure, compliant solutions, including:
» Sustainability & Cost-Efficiency Programs
» Technical Documentation & Compliance Reviews
» Design & Development
» Verification & Validation
» Global Compliance Strategy
» Equipment Process Validation
» CAPA & Root Cause Analysis
» Test Plan Development & Validation
» Asset Delivery for Pharmaceutical Packaging
» Temperature-Controlled Packaging
» Container Closure Integrity Testing (CCIT)
Our programs deliver cost-effective, eco-friendly packaging solutions without sacrificing quality or compliance. By evaluating materials and configurations, NPG helps clients meet both financial and environmental goals, optimizing packaging processes to reduce costs while supporting sustainable practices across medical device and pharmaceutical packaging operations.
NPG provides comprehensive documentation services, including design controls, gap analysis, and annual compliance reviews. Our expertise ensures that both medical device and pharmaceutical packaging remains fully compliant, supporting ongoing quality improvements and aligning with regulatory standards for reliable and consistent market success.
NPG creates specialized packaging solutions for medical devices that ensure sterility, durability, and full regulatory compliance. From initial concept to final validation, our solutions meet stringent industry standards, offering clients reliable, high-quality packaging that enhances product safety and integrity.
NPG’s validation services, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), ensure packaging reliability, safety, and compliance throughout the device lifecycle. Our thorough validation process mitigates risks and guarantees that packaging meets industry standards, supporting smooth product approval and market readiness.
Tailored strategies ensure medical device packaging aligns with US, EU, and global regulations, keeping products compliant, safe, and market-ready. NPG’s expertise in global standards helps clients navigate complex regulatory landscapes confidently, minimizing delays and ensuring regulatory alignment across all operational regions.
We validate both new and relocated equipment used in device packaging, performing rigorous statistical analysis and setup to ensure consistent performance. Our validation process supports operational excellence, guaranteeing that equipment meets quality benchmarks, optimizes productivity, and sustains regulatory compliance.
Using DMAIC methodologies, NPG addresses root causes and implements corrective actions for medical device packaging, optimizing processes and enhancing compliance. Our CAPA services improve operational efficiency, reducing downtime and ensuring robust packaging processes aligned with regulatory standards.
We offer customized testing strategies to ensure packaging integrity, developing and validating methods that meet regulatory and product requirements. From ISO 11607-based packaging integrity tests to tailored procedures, our test plans ensure compliance and reliable evaluations that support safe, secure product delivery.
Specializing in packaging for pharmaceutical equipment like autoinjectors, we support high-speed production setups with top pharmaceutical companies and CMOs. Our expertise ensures efficient equipment line installations, reducing setup times and enhancing production consistency,facilitating reliable market entry for key pharmaceutical products.
For temperature-sensitive pharmaceuticals, NPG’s packaging solutions manage transit conditions to prevent temperature excursions, ensuring product efficacy. We employ robust shipping lane management and validation practices, guaranteeing that products maintain the required temperature throughout transit for reliable patient safety.
Rigorous CCIT validation ensures pharmaceutical packaging maintains sterility and regulatory compliance, especially crucial for injectables and combination products. NPG’s testing safeguards patient safety and supports regulatory alignment, ensuring that all primary packaging meets the highest standards for pharmaceutical integrity.
We leverage NPG's packaging engineering services because we do not have enough experienced staff to handle all aspects in-house, and it would be difficult to build up those internal capabilities. That’s why we utilize NPG’s packaging engineering support as they are experts and save us the time and energy of figuring out things that are out of our area of expertise.
— Specialty Pharmaceutical Client
Director of Packaging Engineering
At NPG, we go beyond packaging solutions; we’re a dedicated partner focused on elevating your projects through compliance, innovation, and strategic insight. Dive into our packaging engineering services for medical device companies and pharmaceutical organizations to discover how we help clients streamline processes, overcome challenges, and achieve measurable results in packaging excellence.
Karen is a motivated, innovative, and growth-oriented professional with over 33 years of experience in Sales & Marketing Leadership and Packaging Engineering. With a proven track record of achievement, Karen is known for her strong leadership skills, the ability to establish positive business relationships, and leading initiatives to enhance performance and increase profitability.
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