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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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

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.

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

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

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.

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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

 
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Tell The Reader More

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Remember:

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

Ready to transform?

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