Pharmaceuticals
Gain unprecedented visibility into pharmaceutical manufacturing operations
Visiv empowers CDMO leaders with an integrated view of manufacturing-related data. See every detail of the production runs, identify potential issues, proactively mitigate risk and optimize operations for maximum efficiency and client satisfaction.

Addressing Challenges in Pharmaceuticals
The growing trend for pharmaceutical companies to outsource drug development and manufacturing to reduce costs, accelerate cycles, and benefit from specialized expertise presents significant opportunities for CDMOs. At the same time, CDMOs face unique challenges:
- Access to Information: Technicians often struggle with overwhelming amounts of data and complex processes, leading to bottlenecks
- Inconsistent Processes: Gaps in training and unclear process requirements creates variability in production runs that undermines operational reliability
- Unidentified Systemic Issues: Limited visibility into recurring deviations and problems hinders proactive problem-solving across the business
- Siloed Operations: Disconnects among manufacturing and other business areas can result in unclear expectations and inefficiencies


The growing trend for pharmaceutical companies to outsource drug development and manufacturing to reduce costs, accelerate cycles, and benefit from specialized expertise presents significant opportunities for CDMOs. At the same time, CDMOs face unique challenges:
- Access to Information: Technicians often struggle with overwhelming amounts of data and complex processes, leading to bottlenecks
- Inconsistent Processes: Gaps in training and unclear process requirements creates variability in production runs that undermines operational reliability
- Unidentified Systemic Issues: Limited visibility into recurring deviations and problems hinders proactive problem-solving across the business
- Siloed Operations: Disconnects among manufacturing and other business areas can result in unclear expectations and inefficiencies

Visiv addresses these challenges by centralizing data, streamlining workflows, and providing insights to help pharmaceutical companies:
- Make smarter, data-driven decisions with visibility into operations, performance and efficiency
- Simplify complex data, uncovering opportunities for improvement and growth without replacing existing systems
- Uncover hidden issues and proactively mitigate risk
- Share understanding across business functions, promoting innovation and differentiation in a competitive market

Visiv addresses these challenges by centralizing data, streamlining workflows, and providing insights to help pharmaceutical companies:
- Make smarter, data-driven decisions with visibility into operations, performance and efficiency
- Simplify complex data, uncovering opportunities for improvement and growth without replacing existing systems
- Uncover hidden issues and proactively mitigate risk
- Share understanding across business functions, promoting innovation and differentiation in a competitive market
Visiv addresses these challenges by centralizing data, streamlining workflows, and providing insights to help pharmaceutical companies:
- Make smarter, data-driven decisions with visibility into operations, performance and efficiency
- Simplify complex data, uncovering opportunities for improvement and growth without replacing existing systems
- Uncover hidden issues and proactively mitigate risk
- Share understanding across business functions, promoting innovation and differentiation in a competitive market

Visiv revolutionizes pharmaceutical manufacturing operations
Visiv Ascent provides a holistic view of drug manufacturing for technicians and leaders, enabling streamlined communication and reporting, confident deviation resolution, rapid risk mitigation, and increased client satisfaction.
With the Visiv platform, companies can customize processes, define KPIs and dashboards and automate report delivery. Simultaneous data input is managed via relational databases, and comprehensive security and audit trails ensure every action is fully traceable. By associating problems and deviations with production runs as they occur, teams can implement data-driven resolutions quickly, identify systemic issues and easily transfer knowledge across sites.
A purpose-built solution for the complex needs of pharmaceutical manufacturing
Visiv Empowers Leaders to Transform Manufacturing Operations with Enhanced Visibility
Proactively Identify and Resolve Issues
Link deviations to equipment, processes, and teams to uncover systemic problems and prevent recurrence.
Streamline Communication and Collaboration
Break down silos with a shared platform for all stakeholders to access real-time data and insights.
Improve Client Satisfaction
Provide clients with greater transparency into production runs and ensure consistent quality control.
Clear & Actionable Data
Cut through the noise—get the right insights at the right time to enhance productivity and compliance.
Seamless Operational Oversight
Connect teams and processes with workflow tracking, ensuring nothing slips through the cracks.
Maximum Efficiency & Growth
Uncover process bottlenecks, optimize resources, and drive continuous improvement across the organization.
Ready to learn more about Ascent?
Download the Product Brief for an overview of key features and benefits.
Visiv Ascent FAQs
We already use systems like MES, LIMS, or QMS. Does Visiv Ascent replace these?
How does Visiv handle compliance with pharmaceutical regulations like FDA 21 CFR Part 11 and GMP?
Compliance is a core part of Visiv’s design. Our platform supports pharmaceutical companies in meeting regulatory requirements like FDA 21 CFR Part 11 for electronic records and signatures, as well as GMP guidelines for manufacturing operations. With built-in audit trails, role-based access controls, and validation-ready reporting, Visiv helps ensure data integrity and regulatory alignment—without adding extra burden for your teams.
How does Visiv ensure the security of sensitive pharmaceutical manufacturing data?
Security is a top priority for Visiv. We use industry-standard encryption for data both in transit and at rest, robust access controls to limit visibility to authorized users, and detailed audit logging to track all activity. Our cloud-based architecture follows best practices for cybersecurity, ensuring that your pharmaceutical manufacturing data is protected while remaining accessible to the right people when they need it.
What if we need to manage a lot of different kinds of information with complex relationships?
That’s no problem. Whether you need to track a handful of business object types or thousands, Visiv is up to the task. With intuitive tooling, defining and modeling business object types and their relationships is simple.
Our IT team is under-resourced or focused on other priorities. Should we wait to consider Visiv?
Not at all. Visiv is specifically designed to empower non-technical users, and it’s quick and simple to implement in your business and integrate with existing IT infrastructure. Visiv empowers non-coders with drag-and-drop tools to build and manage sophisticated web applications based on business logic rather than technical expertise. That said, we also have a dedicated team of experts ready to answer questions, offer advice, and assist with any aspect of building, launching, or managing your application.
This all sounds very simple and user-friendly, but we just don’t have the bandwidth for anything else. Do we have to build our own application?
No. In fact, many Visiv customers choose to implement one of our off-the-shelf applications built to address use cases specific to their industry and ready to deploy without any “build” needed. In addition, if needed, our expert team can help with any or all aspects of bringing Visiv to your business, whether you need support in designing, building, testing, implementing, or managing your application.

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