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    2021 Trends in Quality Management

    2021 quality management trends reports

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    2021 Trends in Quality Management

    2021 quality management trends reports

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    2021 quality management trends reports

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    2021 Trends in Regulatory Management

    2021 quality management trends reports

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    Buyer's Guide for Claims Management

    2021 quality management trends reports

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    Clinical Suite Product Brief

    2021 quality management trends reports

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    2021 quality management trends reports

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    2021 Trends in Quality Management

    2021 quality management trends reports

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    Specialty Chemical Industry Compliance Software Solutions

    Modern Cloud Software for the Specialty Chemicals Industry

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    Challenge Product Innovation Constraints

    Modern Cloud Software for the Specialty Chemicals Industry

    Bring innovative, high quality products to market faster
    without compromising compliance.

    Efficiency, speed and transparency are critical to success in delivering faster innovation to meet the demands of sustainability and circularity.
    Veeva provides modern, easy-to-use, unified solutions for regulatory, QHSE, studies and advertising claims management enabling Specialty Chemical companies to accelerate growth and reduce risk.


    Why you should transform product compliance now

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    CONNECT YOUR
    SYSTEMS

    • Establish a single source of truth for regulatory content and data.
    • Enable intelligent and coordinated
      flow of information.
    • Create user-friendly experiences.

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    CONNECT YOUR
    PROCESSES

    • Streamline and harmonize
      global processes.
    • Design efficient and transparent
      digital workflows.
    • Leverage emerging technologies
      with data

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    CONNECT YOUR
    PEOPLE

    • Improve collaboration with internal
      and external stakeholders.
    • Allocate resources where they create
      the most value.
    • Develop scalable and flexible teams

     

    Founded in 2007, Veeva's cloud solutions are trusted by more than 950+ customers in 165+ countries.

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    Solutions
    Clinical
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    Study Visibility
    Study/Site Planning & Tracking
    Vendor Oversight
    Inspection Readiness

    RegulatoryOne
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    Regulatory Documents
    Dossier Management
    Registrations & Certifications
    Compliance Management

    QualityOne
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    QA/QC, Food Safety
    Document Control & Training
    Supply Chain Collaboration
    HSE Incident Management

    Claims
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    Claims Management
    Localization of Global Claims
    Challenge Response
    Packaging Copy Management

     
    UNIFIED

    Ensure seamless cross functional alignment from supply chain to consumer
    AGILE

    React to changing market realities and
    customer demands with SPEED
    TRANSPARENT

    End-to-end visibility and traceability
    throughout the Product Journey

    Regulatory Management

    Increase customer trust and responsiveness by accelerating Product Stewardship and Regulatory Affairs processes and maximizing global transparency.

    • Accelerate and unify regulatory requests, data and documents
    • Enable global collaboration and coordination
    • Simplify submission and registration management
    • Unlock regulatory insights

    Learn More Download Product Brief Regulatory Transformation Webinar

    Quality and HSE Incident Management

    Improve customer experience by maximizing product quality, ensuring compliance and accessing the digital quality customer voice.

    • Transform feedback and KPIs into product and process insights and improvements
    • Accelerate identification and resolution of complaints, non-conformances and incidents
    • Unify Documents, Training, eQMS and HSE Incidents in a single, easy-to-use application
    • Maximize supplier performance, response and compliance with digital supplier corrective actions, remote audits and automation of CoA inspections.

    Learn More Download Product Brief Transforming Quality and HSE Webinar

    Advertising Claims & Packaging Copy Management

    Ensure global claims compliance by managing the end-to-end process for advertising claims and all elements on a package. 

    • Full detail on permissible usage by product, geography, and marketing channel
    • Workflows for creation, substantiation, review and approval, with audit trails
    • Generate pack copy sheets automatically
    • One click traceability from claim to substantiation and marketing assets using the claim
    • Claim risk ratings with automated prompts and triggers for review workflows

    Learn More Download Product Brief

    Study Management (Veeva Clinical)

    The Veeva Clinical Suite delivers a unified, cloud based solution to manage complex studies. With applications focused on managing study documents, data and processes, as well as tracking payments to sites, company sponsors, CROs, and other study partners can now have full visibility into the process and a single source of truth for all study information.

    • Provides real-time inspection readiness, full visibility into study completeness
    • CRO’s gain the flexibility to efficiently populate studies
    • Manage the entire end-to-end clinical study process and gain a global view into tasks in one unified system

    Learn More Download Product Brief

    Demo Videos

    Regulatory Document Management

     

    Regulatory Document Management

    Stop wasting time looking for documents and data. Accelerate and unify regulatory affairs teams with Regulatory document Management, an intuitive, fit-for-purpose authoring, collaboration and management system that brings efficiency, transparency, accuracy and security to global teams and external stakeholders.

    Watch Demo

     

    Regulatory Supplier Compliance Management

     

    Regulatory Supplier
    Compliance Management

    End-to-end regulatory compliance begins with keeping suppliers accountable for the raw materials they provide. With Veeva RegulatoryOne, you can safely and securely include them directly into your own regulatory processes to drive efficiency, transparency, collaboration and a data-driven regulatory culture. No more email attachments, no missed deadlines. Instead, end-to-end compliance in a single source of truth.

    Watch Demo

     

    Regulatory Request Management

     

    Regulatory Request Management

    Respond to customers and other stakeholders faster and more accurately using Regulatory Request Management. Workflows and automation route requests to the right specialists and preselect relevant response documents dramatically increasing efficiency. Real-time dashboards provide full transparency, KPI tracking and insights for continuous improvement.

    Watch Demo

     
    Customer Success DSM

    Read the DSM Story

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    Watch the Syngenta Interview

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    Tell The Reader More

    The headline and subheader tells us what you're offering, and the form header closes the deal. Over here you can explain why your offer is so great it's worth filling out a form for.

    Remember:

    • Bullets are great
    • For spelling out benefits and
    • Turning visitors into leads.
    Seqens-img-thumnail

    Read the Seqens Story

    Something Powerful

    Tell The Reader More

    The headline and subheader tells us what you're offering, and the form header closes the deal. Over here you can explain why your offer is so great it's worth filling out a form for.

    Remember:

    • Bullets are great
    • For spelling out benefits and
    • Turning visitors into leads.

    What Our Customers Are Saying

    DSM_SimplifiedLogo_SolidWhite

    “Veeva Vault Platform helped us transform and speed up our regulatory processes. It streamlines product submissions and establishes a single source of truth across all stakeholders. It provides us with the needed visibility and helps us increase our productivity.”

    Dr. Landry Le Chevanton, Head of RAQM/Operations at DSM

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    “Over the last three years we moved our entire infrastructure to multi-cloud and best-of-breed SaaS application infrastructure where QualityOne is one major milestone in that. And I think that if we had not done that we would have been in major trouble.”

    Ole Thoreson, Dir. Digitization and Improvements, Aker BioMarine

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    "To sustain compliance across sites worldwide, Seqens needed a robust and flexible cloud solution for managing Quality events. For this reason, we chose Veeva as our preferred digital quality solution. It started first with document control, CAPA, Deviation and Notification to management and now it’s expanding to OOS. We plan to implement additional quality events in the foreseeable future. The flexibility of Veeva QualityOne enables us to adapt it to meet our requirements."

    Stéphanie GIRARD, Global Quality & Regulatory Director, Seqens

    Resources

    Webinar

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    Chemical Coffee Talk Series - Regulatory Transformation in Chemicals

    Webinar

    Webinar Circular Economy

    The Circular Economy Data Challenge

     

    2021 Trends Reports

    2021 Trends in Quality Management

    2021 Trends in Quality Management



    Ready to transform?

    Improve your agility, transparency, and compliance with Veeva's Cloud solutions for
    regulatory, quality, advertising claims, and clinical management.

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    About Veeva Systems

    Founded in 2007, Veeva NYSE (VEEV), is a global provider of industry-specific cloud software solutions that address the unique operating challenges and regulatory requirements of the consumer products and chemical industries. Our solutions help R&D, quality, regulatory and commercial teams eliminate inefficiencies and bring high-quality, safe, sustainable products to market without compromising compliance. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America. Read Our Story

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