We empower our clients with streamlined, tailored labeling solutions for seamless operations.
Our labeling services offer comprehensive capabilities powered by advanced AI, expert-driven compliance, and adaptable consulting and staffing solutions. Acting as an extension of your team, NPG manages complex global systems, regulatory needs, and daily label changes with unmatched precision and efficiency, supporting both consulting and surge capacity.
NPG accelerates product readiness with NPG’s labeling expertise, ensuring secure, compliant solutions, including:
» Day-to-Day Label Changes
» Format Migration
» Label Parsing and Verification
» Global Labeling System (GLS) Implementation
» Software Validation
» Creation Activities
» Data Migration
» Instructions for Use (IFUs) & Electronic IFUs
» Label Template Creation
» Graphic Design Services
» Clinical Trial Labeling Support
NPG handles daily label updates with precision, offering surge capacity to maintain efficient operations. Our Team manages each change order meticulously, ensuring thorough documentation within your systems, supporting compliance, accuracy, and smooth functionality for ongoing labeling needs.
We specialize in migrating legacy labeling systems to modern formats, preserving document integrity and enhancing usability and functionality. Our process ensures a seamless transition, supporting regulatory compliance and improved document accessibility, aligning with current industry standards for life sciences labeling.
With our advanced tool, FALCON, NPG parses and verifies label changes swiftly, enhancing accuracy and reducing error rates. This tech-enabled solution automates verification, ensuring precise compliance with regulatory standards and supporting seamless, efficient updates across labeling workflows.
Through a structured seven-step process, clients are guided from initial GLS validation to deployment, ensuring regulatory compliance at every phase. NPG’s method integrates efficiently across workflows, supporting seamless global labeling system implementation that aligns with industry standards and minimizes operational disruptions.
Following the V-Model framework, this turnkey validation service ensures that each stage of your software lifecycle is documented and compliant. Every critical validation step is addressed to maintain accuracy, reliability, and regulatory standards, preparing your systems for dependable and compliant operation.
NPG supports the development of User Requirement Specifications (URS) and essential risk documentation with a focus on compliance and traceability. Our structured approach ensures every requirement is met accurately, helping you establish a solid, regulatory-ready foundation that aligns with industry standards and provides a reliable blueprint for your project.
Managing the full migration of labeling data from legacy to updated formats, NPG ensures data accuracy and regulatory compliance throughout. This careful process provides a seamless transition to modernized labeling platforms, giving you improved functionality and easier data management without compromising essential compliance standards.
Our team develops and updates IFUs and electronic IFUs, streamlining processes to ensure regulatory compliance and easy accessibility across platforms, including Qurad. We ensure labeling meets current standards, enhancing usability and supporting seamless global distribution.
We design customized labeling templates that ensure consistency and regulatory compliance across all products, adaptable to various Global Labeling Systems. NPG templates are tailored to meet specific regulatory needs, streamlining the labeling process and supporting accuracy, brand consistency, and global alignment.
NPG’s graphic design team creates visually engaging, regulatory-compliant labels that enhance clarity and ensure the effective communication of essential information. Our experts specialize in combining aesthetics with functionality, supporting product usability and aligning with industry standards for life sciences labeling.
Our Clinical Trial Labeling Support offers on-demand label creation, allowing rapid adaptation to evolving requirements while maintaining strict compliance with regulatory standards. We ensure that labels meet precise specifications, supporting accuracy, regulatory alignment, and flexibility throughout the clinical trial process.
Working with NPG’s labeling team feels like they’re part of our own. They access our systems remotely, handle updates efficiently, and seamlessly collaborate with us, providing expert support without additional on-site staff.
— Mid-sized Pharmaceutical Client
VP, Regulatory Services
At NPG, we’re more than labeling experts; we’re a committed partner in delivering accuracy, compliance, and innovative solutions. Explore our labeling videos case in our resources to see how we’ve helped clients navigate global requirements, enhance product traceability, and achieve reliable, compliant labeling that drives success.
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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