Validation, Commissioning & Design Products & Services
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Labeling System For Folding Boxes: HERMA 362E TE
12/11/2024
The 362E TE is a versatile labeling machine that prioritizes safety and efficiency, ensuring accurate and tamper-evident labeling of folding boxes while maintaining rigorous quality control.
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Compliance & Regulatory Programs For Drug Manufacturing
10/25/2024
Our experts implement proven, streamlined processes that maintain compliance, quality standards, and efficiency while also managing costs, schedules, and scope.
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Pharmaceutical Digital Transformation & Harmonization Programs
10/24/2024
Life Sciences companies are frequently slowed by siloed departments, outdated technologies, and stalled communications between office locations. Streamline operations while enhancing your tech stack to deliver speed, flexibility, and scalability to every project.
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Pharmaceutical Operational Readiness Programs
10/24/2024
Many Life Sciences companies struggle to minimize downtime, ensure safe operations, and reach tight production schedules while maintaining consistent, quality output in a demanding environment, but you can boost efficiency and reliability through our field-tested methodologies.
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Phase 1, 2, And 3 Clinical Supply
10/23/2024
Upperton provides clinical supplies for Phase 1, Phase 2, and Phase 3, specializing in oral, nasal, and pulmonary dosage forms.
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Digitally Enhanced Cleaning And Validation
10/21/2024
As the time, costs and complexity of cleaning validation challenges grow, savvy life sciences companies are building a competitive advantage around smarter approaches to cleaning validation.
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Quality Management System (QMS) For Drug Manufacturing
9/19/2024
The #1 QMS In Life Sciences Puts You in Complete Control
MasterControl Quality Excellence is trusted by 1,100+ customers — from startups to global enterprises — to bring quality products to market faster.
It's time to close the loop on quality—from quality event management to document management and training—and see how MasterControl quality management system can transform your business today.
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Meet The Most Effective QbD Implementation Platform
8/6/2024
Spreadsheets don't belong in your QbD process. Discover the ValGenesis iRisk platform that has a single repository to ensure easy access to your data, seamless data transition, smart detection for your areas of concern, and assessment reusability.
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It's Time To Abandon Spreadsheets For QbD
8/6/2024
Ditch the spreadsheets, and dive into efficiency. Seamlessly integrate QbD principles and risk management practices into your pharmaceutical development process.
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Reduce The Burden Of Software Validation Testing
8/6/2024
Are you bogged down by the endless protocols and documentation CSV requires? Do you feel overwhelmed by exhaustive testing but unsure of how to implement CSA?