ABOUT VEEVA
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world’s largest biopharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves.
FEATURED ARTICLES
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Explore common misconceptions that obstruct progress and why overcoming these barriers early provides a competitive edge when preparing for commercialization.
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Learn how one CDMO successfully streamlined and modernized its QC workflows and processes to address challenges related to the increasing demand for cell and gene therapy manufacturing services.
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Conventional QC workflows often involve manual data entry and transfer, which can result in errors. Learn how one partnership is seeking to streamline and unify data management in QC.
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Explore a framework demonstrating the value of adopting a digital, data-centric approach to validation management to executives and stakeholders.
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Business leaders can enhance QC operations by adopting a holistic view of the quality ecosystem and embracing comprehensive modernization strategies. Explore four principles for greater QC lab agility.
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Discover the best way to successfully modernize QC laboratories.
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See how one company was able to connect its quality processes, improve collaboration across business functions, and address the needs of its digitally-aware workforce.
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Learn how a global CDMO improved efficiency, visibility, and collaboration by standardizing quality procedures and expanding them to external partners.
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Explore a quality reference model that aims to foster further standardization within the life sciences industry, and discover the advantages of leveraging the standardized best practices within.
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Here, we outline a holistic approach to streamline the change control process, aiming to increase efficiency and compliance, improve quality, and shorten time-to-market.
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Here, we outline a holistic approach for CDMOs to streamline the change control process, aiming to enhance quality, compliance, and time-to-market.
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Learn how to overcome the hurdles associated with traditional data management approaches, and discover the key to reducing the risk of drug shortages in pharmaceutical manufacturing.
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Discover the key to a successful quality transformation, explore the business value of modern quality systems, and learn how quality leaders can build a compelling case for change.
CONTACT INFORMATION
Veeva
4280 Hacienda Drive
Pleasanton, CA 94588
UNITED STATES
Contact: Nicole Connell
FEATURED PRODUCTS
FEATURED VIDEOS
- A Digital Solution For Validation Management
- Why Use A Modern Laboratory Information Management System?
- A Unified Laboratory Information Management Systems (LIMS) Solution
- A Quality Management System For Ensuring Inspection Readiness
- Optimize QC Labs To Increase Right First Time And Reduce Complexity
- Training Solutions To Optimize Quality And Compliance
- AI Myths Vs. Reality In Quality
- Streamlining Content Management And Training With Vault Quality
- Streamlining Change Control With Unified Quality