Validation, Commissioning & Design Products & Services

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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?

  8. Should You Digitalize Your CQV Process? 8/6/2024

    Legacy paper trails are a compliance nightmare.

    Missing documents, illegible handwriting, and inconsistent data leave you scrambling and vulnerable during audits. Digital CQV captures data and objective evidence in real time, ensuring a crystal-clear audit trail with time-stamped entries and electronic signatures that meet 21 CFR Part 11 requirements.

  9. Leave Paperwork Behind In Your CQV Process 8/6/2024

    ValGenesis VLMS: The Industry-Leading Platform For Digital CQV

  10. Digital Validation Lifecycle Management Software 7/10/2024

    The leader in digitizing validation

    Setting the digital validation standard for 20 years, ValGenesis VLMS is used by 30 of the top 50 global life sciences companies.

    The gold standard of standardization

    Strengthen your compliance stance and lower the cost of quality with enforced standardization and absolute data integrity.

    Knowledge integrity to data integrity

    Gain total peace of mind with a single source of validation truth with documentation aligned to ALCOA+ standards.

    One platform, boundless scale

    Start small or start global. VLMS scales effortlessly to support new systems, new sites, new products, new languages, and new validation processes.