Veeva Updates: 26R1 Release Highlights

Veeva Updates: 26R1 Release Highlights

Veeva continues to deliver enhancements to its platform through three structured releases each year. It is critical for the administrators of Veeva solutions to review each new update to assess new capabilities, align priorities, and prepare their environments for any technical or functional changes.

fme’s specialists review each release in detail to identify changes that may impact our clients’ environments, and highlight new capabilities that can improve efficiency, compliance, and overall system performance. Here are summaries from past releases:

In this installment, we describe key highlights from the 26R1 Update to help you quickly understand the most relevant changes. Please note that this is not a comprehensive list of changes; please visit Veeva’s site for the complete details and descriptions.

For a deeper analysis or to discuss how fme can support ongoing optimization of your Veeva environment, we invite you to download our service datasheets below and schedule a time to connect with our team.

Key Feature 1: Milestone Object Model

Staring in 26R1, milestones are no longer stored as a single field (milestone__v) but are managed as object records. The new object model is more scalable and aligns with Veeva’s overall data structure approach.

Each milestone (Approved, Effective, Submitted, etc.) is now tracked as its own entry instead of being grouped in one place, allowing users to view all milestones in a dedicated Milestones panel on the document. In addition, the 1,000-record limit within the milestone__v field has been removed.

This change can affect existing reports, integrations, or configurations that reference the milestone field, and administrators may need to make adjustments to reflect the new object.

How this can benefit customers

There are several benefits to these changes:

    • Multiple milestones can be stored and managed more clearly for each document and version within the version tree.
    • The new structure makes it easier to understand the full lifecycle history of a document.
    • Each milestone is now its own record that can be queried and analyzed significantly improving reporting on milestones.
    • Admins can now filter, group, and report on milestones across documents more easily than before.
    • This change also supports more complex use cases, such as tracking multiple milestone types or repeated events over time.

Key Feature 2: Doctype Triggers (Automation)

Prior to 26R1, actions required when a document was created, updated, or deleted were mostly a manual process with minimal automation available. The 26R1 release allows users to attach triggers with logic directly to documents so that when the trigger is fired, Vault instantly runs custom actions behind the scenes.

This feature can significantly reduce the amount of manual work users have to perform, reduce human error, make processes faster, and allow admins more opportunities to customize document behavior.

How this can benefit customers

One possible application of this new feature is to auto-populate specific fields when creating documents. For example, when a user is creating an SOP, triggers can auto-populate the product, region, and department within each unique SOP template ensuring accuracy and consistency.

In Veeva PromoMats (Promotional Materials), a newly created promotional piece can automatically link required objects, like products or specific campaigns, greatly accelerating content creation while also reducing compliance risk. A trigger can also be created to automatically assign a document for training when it becomes approved/effective.

Key Feature 3: Excel Copy/Paste

The reality of modern business ensures we will almost always work with spreadsheets, and prior to 26R1, users had to add each value manually. With the 26R1 release you will be able to copy a list of values from Excel and paste them directly into Vault instead of entering them one by one.

How this can benefit customers

This update eliminates repetitive, manual data entry saving time, minimizing copy/paste errors, and greatly accelerating the input of large lists of values. It is especially useful when working with multi-value fields, such as users, products, or countries. Instead of manually searching and selecting each value, you can paste an entire list in a single action. Vault automatically recognizes and matches the pasted values to existing records or picklist values.

Veeva Vault will automatically ignore duplicate values, preventing accidental double entries. If any values don’t match, Vault provides a summary so you can quickly identify and fix issues.

This makes bulk updates much faster without needing loaders or external scripts, and brings a more familiar, Excel-like experience into Vault to improve usability for everyday users. With this update, expect a significant reduction in manual errors and user frustration caused by repetitive manual data entry.

Key Feature 4: API Endpoint Deprecation

Not all changes are adding features. With the 26R1 update the “Retrieve All Documents” and “Retrieve all Binders” APIs are no longer supported. In the past, this was used to pull large sets of documents in one go causing heavy system load and slowing down Vault performance. Instead, users are now expected to use VQL (Vault Query Language) to retrieve only the data they need.

To prepare for this change, administrators should replace existing “Retrieve All Documents” and “Retrieve All Binders” API endpoints with VQL queries.

How this can benefit customers

Basing their decision on industry best practices for data access, Veeva made this shift to improve system performance and scalability, and to encourage more efficient, targeted data requests based on document type, specific dates, statuses, etc. rather than full data extracts.

fme’s dqMan has a Veeva Vault Edition that can be a great help in this change. It is a professional administration tool based on VQL and MDL, providing users with exclusive capabilities and a broad feature set to help manage Veeva Vault applications efficiently. Contact us to learn more.

How fme Can Support Your Veeva Updates

Veeva’s innovation-driven release cycles provide continual improvements, but also require ongoing operational responsibility. Releases occur on a fixed schedule, regardless of internal IT bandwidth or competing priorities, and certain changes are deployed automatically. Configuration shifts, deprecated settings, and legacy customizations can all affect how new functionality performs within a given environment.

fme provides tailored services to help clients evaluate, manage, and operationalize Veeva’s recurring release cycles. Below are two core offerings our clients rely on to keep their Veeva environments optimized and aligned with evolving business needs.

HealthCheckAssist: Gain Visibility and Control

HealthCheckAssist is a structured, low-burden assessment designed to provide actionable insights into your Veeva RIM environment. We evaluate how the system is configured and used, identify active risks and inefficiencies, and highlight opportunities for optimization.

Beyond diagnostics, we deliver a prioritization remediation roadmap clearly outlining the steps required to stabilize, streamline, and future-proof your environment. This enables your team to proactively prepare for upcoming releases, fully leverage new platform capabilities, and maintain a consistently release-ready experience.

Learn more about HealthCheckAssist now!

TechOps Support Services: Cost-effective Platform Management

Efficient and effective IT operations are vital for any company but are notoriously difficult to accurately predict and budget for, especially in multi-platform systems. Our TechOps Support Services provide the experience and resources needed to augment and support the needs of complex IT environments, balancing out the ebb and flow of support tasks, and adding extra knowledge and skill for integrated application management.

Our flexible, customizable model can incorporate administrative support and release management components to allow your organization to focus on your core business activities without the distractions of technical issues and system maintenance.

Our trained experts support many legacy and modern applications to ensure your critical systems remain stable and secure, giving them the attention they need while you focus on accomplishing your business goals.

Learn how fme can simplify your platform management with TechOps Support Services now!


About the Author

Matthew Peterson

Matthew Peterson is a highly skilled Veeva business analyst and migration specialist at fme, focused on helping clients understand how each Veeva update will impact their environments. With deep expertise in the intersection of technology, data, and regulated life sciences processes, Matthew ensures that clients not only stay current with platform changes but also align those changes with their strategic goals and operational priorities. His commitment to clarity and practical impact helps organizations maintain optimized, resilient Veeva implementations that support long-term success.

 

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Copenhagen is Around the Corner: Veeva R&D Summit Europe

Copenhagen is Around the Corner: Veeva R&D Summit Europe

Veeva R&D Summit Europe is only a few short months away, and fme’s experts are preparing to share how we help organizations harness the full power of Veeva to enable digital transformation and long-term growth. With its unified suite of applications, Veeva serves as a strategic hub for regulated content and data, designed to improve collaboration, strengthen compliance, and accelerate speed to market.

Realizing that value, however, depends on more than platform configuration alone.

Data as the Critical Enabler

Like any enterprise technology solution, the success of Veeva is directly tied to the quality, structure, and regulatory integrity of the data it manages. To unlock the full capability of the platform, data must be accurate, complete, governed, and migration-ready from day one.

For life sciences organizations, this is a complex and high-stakes undertaking. Fragmented repositories, inconsistent metadata, missing lineage, and stringent GxP validation requirements introduce risk that can delay transformation and increase compliance exposure.

To reduce risk and ensure long-term platform value, your migration approach must be:

  • Governed and accountable, with defined ownership, stewardship, and documented business rules
  • Profiled and transparently assessed, identifying completeness gaps and cross-object dependencies
  • Systematically remediated and standardized, aligned to controlled vocabularies and target-state metadata models
  • Validated within GxP- and CSV-aligned frameworks, with full traceability and audit-ready documentation

By addressing these elements proactively, organizations position Veeva to deliver sustained regulatory confidence and measurable operational value.

Trusted for the Industry’s Most Demanding Migrations

Delivering value on Veeva requires proven execution in complex, regulated environments.

fme supports large-scale Vault migrations involving millions, and in our most recent cases tens of millions, of documents and records, executed under compressed timelines and strict compliance requirements. Our methodology is tailored to each organization’s operating model, regulatory landscape, and technical architecture, whether deploying globally or through phased rollouts.

By combining structured Data Readiness with Veeva-certified accelerators like migration-center® and our AI-assisted MetadataAssist℠ engine, we ensure governed, validated, and migration-ready data, enabling a controlled, compliant transition to Vault.

With fme, you gain a strategic partner focused on long-term platform success, not just system go-live.

Ready to explore your path to Veeva?

Before you travel to the Veeva R&D Summit Europe in May, download our Veeva capabilities overview below to learn more about our services, tools, and client success stories. Then, we’ll schedule a discovery meeting where we’ll discuss your current environment (or environments) and walk through the next steps for accelerating your Veeva transformation.

Veeva Updates: 2025 Release Summary

Veeva Updates: 2025 Release Summary

Each year, Veeva updates their platform in three scheduled releases: April, July, and December. Approximately one month before each release, upcoming changes are announced to ensure administrators have adequate time to review, plan, and prepare for the coming improvements and modifications. Some changes are technical fixes with limited visible impact, while others introduce new features and functionality that clients have requested or they have developed in support of ever-evolving regulations as well as innovation. There can also be under-the-hood technical changes that require configuration adjustments or administrator preparation to allow for a seamless update.

For each release, fme’s experts receive the official announcements and distill the updates into a clear, client-focused summary. This includes outlining the changes that will impact their environments while highlighting new capabilities that could enhance their internal workflows and business processes.

Below we’ve summarized selected highlights from Veeva’s 2025 updates, and how these changes can benefit Veeva Vault users. This overview is not exhaustive. If you would like a deeper dive into the updates, or to explore how fme can help you analyze, monitor, and optimize your Veeva environment to keep it as performant as possible, download the data sheets below and contact us to discuss your current challenges.

Veeva Update 25R1 – April 2025

25R1 Key Feature

One of the more interesting elements in this release is how Veeva updated their functionality for collaborative authoring. Previously, you only could @mention users who clicked “Edit in Microsoft Office” in Vault. With this release, users are now allowed to automatically add workflow participants to the document being edited in SharePoint upon checkout in Vault, so they can be @mentioned immediately.

How this can benefit customers

Collaborative Authoring makes it much easier for teams to work on the same document at the same time without juggling emailed copies or tracking down the “latest version.” This change will speed up authoring and review cycles, reduce potential version confusion, and help teams keep content consistent when multiple stakeholders need to contribute.

Veeva Update 25R2 – July 2025

25R2 Key Feature

In this release Veeva introduced “Action Triggers”, a simple way for admins to automate actions when object records change (create/update/delete). Action Triggers reduce the need for custom SDK trigger development and can be managed through the configuration.

Action Triggers are simple “IF/THEN/ELSE” statements that can be created both before and after events for the “Create/Update/Delete” operations. They can also automatically enforce rules and populate standardized values. For example:

  • Auto populate fields based on metadata
  • Automatically set record status (Draft to In Review) when specific required fields are completed

How this can benefit customers

Action Triggers can be helpful during migrations because it can automatically handle key next steps, like updating fields, starting workflows, or creating related records as soon as the migrated data hits certain conditions. This means less manual cleanup after the load and more consistent processing, so clients can go live faster with fewer surprises later on.

Veeva Update 25R3 – December 2025

25R3 Key Feature

In this release Veeva introduced an improved multi-Vault user experience, allowing users to login and work across multiple Vaults at the same time. Prior to 25R3, the user would be logged out from one of the sessions, but now they can stay logged in when switching between the two.

How this can benefit customers

This feature is particularly useful since it allows users to be logged into both source and target vaults at the same time in one browser. This makes it much faster to compare records, confirm mappings, and validate migrated content during migrations between Vaults. It also reduces constant logouts and re-authentication, helping migrations run more efficiently with fewer user errors and quicker issue resolution.

Get the Full Release Details

For complete details on all Veeva updates, visit their site here, or contact fme below to schedule a discussion focused on your unique platform and requirements.

How fme Can Support Your Veeva Updates

Veeva’s SaaS delivery model has long provided clients with predictable, innovation-driven release cycles. However, that same continuous update cadence introduces an ongoing operational responsibility. Releases occur on a fixed schedule, regardless of internal IT bandwidth or competing priorities, and certain changes are deployed automatically. Configuration shifts, deprecated settings, and legacy customizations can all affect how new functionality performs within a given environment.

Even incremental updates can have downstream effects: missed capabilities, user friction, reporting inconsistencies, or reduced process efficiency. Sustaining ROI in a mature SaaS platform requires structured review, impact analysis, and proactive configuration management throughout the year, not just at go-live.

fme provides tailored services to help clients evaluate, manage, and operationalize Veeva’s recurring release cycles. Below are two core offerings our clients rely on to keep their Veeva environments optimized and aligned with evolving business needs.

HealthCheckAssist: Gain Visibility and Control

HealthCheckAssist is a structured, low-burden assessment designed to provide actionable insights into your Veeva RIM environment. We evaluate how the system is configured and used, identify active risks and inefficiencies, and highlight opportunities for optimization.

Beyond diagnostics, we deliver a prioritization remediation roadmap clearly outlining the steps required to stabilize, streamline, and future-proof your environment. This enables your team to proactively prepare for upcoming releases, fully leverage new platform capabilities, and maintain a consistently release-ready experience.

Learn more about HealthCheckAssist now!

TechOps Support Services: Cost-effective Platform Management

Efficient and effective IT operations are vital for any company but are notoriously difficult to accurately predict and budget for, especially in multi-platform systems. Our TechOps Support Services provide the experience and resources needed to augment and support the needs of complex IT environments, balancing out the ebb and flow of support tasks, and adding extra knowledge and skill for integrated application management.

Our flexible, customizable model can incorporate administrative support and release management components to allow your organization to focus on your core business activities without the distractions of technical issues and system maintenance.

Our trained experts support many legacy and modern applications to ensure your critical systems remain stable and secure, giving them the attention they need while you focus on accomplishing your business goals.

Learn how fme can simplify your platform management with TechOps Support Services now!


About the Author

Matthew Peterson

Matthew Peterson is a highly skilled Veeva business analyst and migration specialist at fme, focused on helping clients understand how each Veeva update will impact their environments. With deep expertise in the intersection of technology, data, and regulated life sciences processes, Matthew ensures that clients not only stay current with platform changes but also align those changes with their strategic goals and operational priorities. His commitment to clarity and practical impact helps organizations maintain optimized, resilient Veeva implementations that support long-term success.

 

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Modernizing Quality: Why Migration Expertise (and the Right Platform) Matters

Modernizing Quality: Why Migration Expertise (and the Right Platform) Matters

Are you still relying on legacy QMS platforms built decades ago? I’m talking about systems that now require constant maintenance (or constant calls to support), rely on outdated architectures, and create operational silos. What once felt “best-of-breed” now limits your ability to support modern quality processes, enable AI-driven insights, or keep pace with today’s evolving regulatory landscape.

Quality expectations have always been rigorous, but they are expanding at a pace that I have not seen, well, ever, and that’s because technology is evolving faster than ever. Organizations need connected, digital ecosystems that deliver agility, compliance, and real-time intelligence across the enterprise. And that starts with rethinking the foundation of your QMS.

The Reality of Migrating to a New QMS

Migrating to a new QMS is one of the most significant transformations a life sciences organization can undertake. It’s not a lift-and-shift exercise. Every repository has its own history, every process has been customized over time, and every record (along with their audit trails!) must be migrated accurately and with full traceability.

There are several modern QMS platforms available today. Some offer strong “QMS-only” capabilities with integration options that can work well for organizations willing to manage multiple systems.

But if your goal is a truly unified quality experience, one that connects processes, content, data, training, labs, and decision-making, after seeing the rapid evolution of it at the last two Summits I attended, Veeva Quality Cloud stands apart. It brings the entire quality ecosystem together in a way integrations alone simply cannot.

Choosing the right platform is important. Choosing the right migration partner is essential.

Why QMS Migrations Demand fme Expertise

QMS migrations are uniquely complex. Beyond moving documents and metadata, they require a deep understanding of:

    • Quality processes and regulatory expectations
    • Legacy data structures, customizations, and usage patterns
    • Veeva’s data model, capabilities, and best practices
    • Organizational change, user adoption, and long-term system health

To achieve a truly successful transformation, you need a partner that considers the entire end-to-end ecosystem, not just the migration task. This is exactly where fme excels.

fme Delivers End-to-End Quality Transformation

Our services and accelerators are designed to support every phase of your quality modernization journey, whether you’re selecting a new QMS, migrating your legacy footprint, or optimizing your Veeva environment post go-live.

Phase 1: Strategy & Evaluation

Start with clarity and confidence.

    • Data Readiness & Governance
      Identify data quality risks, inconsistencies, and structural issues early, ensuring a clean, compliant, business-aligned migration.
    • SelectAssist℠ for Quality
      Choosing a platform is complex. Leverage our experience to evaluate your needs and identify the best-fit Quality solution.
    • Migration Readiness Evaluation
      Gain a comprehensive understanding of your current data, documents, and system landscape to reduce migration risks, minimize internal effort, and plan effectively.

Phase 2: Migration

Where strategy becomes execution.

    • MetadataAssist℠
      Use our AI-powered accelerator to classify, clean, and enrich content that’s been fragmented through years of upgrades, consolidations, or manual processes.
    • Migration Execution
      Our deep technical expertise ensures seamless, compliant migration—mapping your business processes to Veeva’s architecture for long-term success.
    • migration-center®
      Our industry-leading migration software delivers efficiency, auditability, transparency, and minimal downtime. Certified by Veeva and proven across millions of documents since 2016.

Phase 3: Stabilization & Optimization

Ensure your Veeva environment grows with your business.

    • TechOps Support Services
      Monitor, maintain, and optimize your Veeva environment—across daily operations and continuous product upgrades.
    • HealthCheckAssist℠
      Assess how your organization is using Veeva and identify opportunities for optimization, remediation, and future scalability.
    • Archiving & Decommissioning
      Preserve historical content securely and compliantly as part of a modern information governance strategy. We just helped a top 10 pharmaceutical company archive 90,000,000 documents. That’s a lot.

fme is the Quality Partner You Can Trust

Every day, we focus on enabling quality excellence for our clients. The world’s leading life sciences firms trust fme with their most complex quality, regulatory, and clinical transformations. We deliver to the same high standards they follow, holding ISO/IEC 27001 QMS and ISO 9001:2015 certifications.

Your quality data is too important to leave to chance. Download our datasheet below to explore fme’s end-to-end Veeva capabilities and see how our expertise can guide your transition.

Ready to talk through your specific challenges?

Our experts are here to help you build a migration strategy that ensures data integrity, compliance, and business continuity—while setting your organization up for long-term success.

About the Author

Meghan is the Vice President of Commercial Operations at fme and an expert in global digital transformation within the Life Sciences industry. She has deep Quality domain acumen along with demonstrated expertise in program governance and account management, consistently driving innovation and delivering measurable results. Meghan has been instrumental in guiding some of the world’s largest pharmaceutical and medical device organizations on their digital journeys, ensuring success through strategic vision, cross-functional collaboration, and a deep commitment to the Life Sciences industry’s needs.

 

Upgrade and Optimize OpenText Solutions for Success in 2026

Upgrade and Optimize OpenText Solutions for Success in 2026

OpenText has been a cornerstone of content management platforms for Life Sciences, Finance, Manufacturing, Automotive, Retail, Insurance and more for decades, delivering unrivaled stability and capability in the most demanding, business critical environments. As we head into 2026, they continue to push the industry forward, upgrading proven core technology and integrating advanced AI-driven capabilities.

To ensure you get the full benefits of your OpenText investment, there are several key areas to consider for both short- and long-term initiatives. Here are a few of the most important.

OpenText Product Lifecycles

The heyday of isolated, on-premises software applications installed on local servers is long gone, evolving into today’s cloud-based, integrated, and always advancing solutions. For better or worse, those improvements can happen fast. Any upgrade can include valuable improvements as well as critical changes that can impact your team and business workflows. Keeping up with changes in capabilities and their deeper impacts has become a continual frustration for IT departments maintaining multiple systems and integrations across complex business environments.

It’s essential to understand which versions are active and vendor-supported to avoid additional maintenance costs and unintentionally paying extra to support obstacles to future innovation. fme keeps close tabs on OpenText’s product lifecycle matrix and works with our clients informed of the critical dates for their individual technology stack.

We also have advanced TechOps Support Services for cost-effective release and application change management, and day-to-day application support if required.

Optimize OpenText Solutions for Your Business

As with any technology, it’s vital that your platforms support your unique business needs and goals. Over our 25 years, we’ve served as our clients’ technology partner, providing an objective perspective to help maximize their technology ROI and minimize their total cost of ownership, balancing costs, capabilities, and business priorities. Learn more in this post where we compare both the benefits and challenges of OpenText solutions, and outline a variety of strategies that provide quick-win and foundational improvements. We can provide a clear roadmap that can both reduce costs and increase efficiency within teams and across departments.

Ensuring System-wide AI Readiness

We are in the middle of a dramatic change in human-software interaction, and the technology hype-cycle is giving way to the real possibilities and applications of AI technology. Regardless of what system or platform you choose, it’s essential that the data and documents fueling your AI platform are organized and ready for ingestion and analysis.

To quote our CEO Dirk Bode, “All the AI in the world won’t help if your data’s a mess. You’ve got to have a solid foundation.” 

fme’s history of content management and platform services gives us an unparallelled understanding of the best practices required to prepare structured and unstructured data for AI solutions.

Let’s Meet at OpenText World!

fme has been an OpenText partner for over two decades and every year we look forward to the announcements, innovations and excitement of OpenText World November 17-20 in Nashville, Tennessee. We will have multiple team members on site to discuss everything OpenText, and to share how fme guides their clients to get the most value from their OpenText solutions. If you are attending let us know below, we’d love to meet you there!

Learn More About fme’s OpenText Solutions

With 25 years of experience, fme has the knowledge and skills to help you maximize the ROI of your content management solutions like OpenText Documentum and OpenText Content Suite. We are the right partner with experience in complex Life Science data, the industry’s leading platforms and the current best-practices and strategies to get the most from the OpenText IT landscape. Let us help you reduce costs while improving your system efficiency and capability.

Webinar 🖥️ Modern Archiving for Life Sciences Enterprises: A Case Study

Webinar 🖥️ Modern Archiving for Life Sciences Enterprises: A Case Study

IT and Operations teams that complete digital transformation programs often face a familiar question: what happens if they decide to leave some records or documents behind? Our clients sometimes run multi-year initiatives to move onto new, best-of-breed platforms. But they may not want to bring every document or decade’s worth of data with them. Still, compliance requirements mean that historical content can’t simply be ignored. So then what? Keep the old systems running? Pay a small team to maintain them?

In today’s competitive environment, these challenges aren’t just operational, they can create a real strategic disadvantage. Let’s look at the most common pain points we hear from clients and partners.

Technical and Operational Challenges

Rising Infrastructure Costs
Maintaining outdated systems and on-premise architectures drives up costs. Hardware upkeep, security patching licensing, and support all add up, making it difficult for organizations to scale efficiently.

System Complexity and Maintenance Overhead
Years of customizations, patches, and integrations often leave legacy platforms fragile. Specialized skills are required to keep them running, but those skills are harder to find as IT professionals gravitate toward modern technologies.

Data Silos and Inconsistent Metadata
Mergers, acquisitions, and department-level repositories often leave organizations with fragmented archives. This leads to inconsistent metadata and taxonomies, reducing visibility and slowing access to critical records.

Compliance and Risk Management Challenges

Audit and Inspection Readiness
Regulators expect rapid, accurate access to historical documents. Legacy systems, with clunky user interfaces and inconsistent metadata, make it difficult to retrieve information quickly during audits or inspections.

Validation Burden
Maintaining compliance requires frequent re-validation of legacy platforms. However, even minor patches or upgrades can trigger new rounds of validation driving up costs and eating up time.

Security Vulnerabilities
Outdated platforms often lack modern safeguards such as role-based access controls, real-time monitoring, or advanced encryption. This leaves sensitive records exposed to potential breaches.

The Bottom Line

IT and Operations leaders are being pulled in all directions: rising infrastructure costs, growing compliance demands, user frustration, and leadership pushing for innovation and AI adoption.

But there is a path forward. Modern archiving strategies allow organizations to move to new platforms without dragging along every last document, while still ensuring compliance, security, and accessibility.

Case Study: fme Modernizes Archiving for Life Sciences Firm

Does this sound familiar? If so, you’re not alone, and there are clear paths forward. There are practical strategies to break free from legacy systems and move toward scalable, secure, and compliant information management.

Early in 2025, one of our global pharma clients faced this exact situation. They decided it was time to retire their costly legacy systems and replace them with a modern archiving solution that could meet today’s business and regulatory requirements.

They turned to fme Life Sciences for our decades of experience in content migrations and our deep understanding of Life Sciences business requirements. Together with our partner Generis, we combined the flexibility of the CARA Platform with the power of fme migration-center to provide a scalable, cost-efficient archiving solution that not only addressed immediate challenges but also laid a strong foundation for future AI-enabled capabilities.

View the Recording to Learn More

If you are struggling with similar challenges with the costs and barriers of legacy systems, view the recording for Modern Archiving for Life Sciences Enterprises: A Case Study to learn more about this distinctive solution. fme’s president Frank D’Entrone and Generis’ Rex Harrison will be sharing details on the project, as well as how the combination of fme and Generis solutions enabled the client to not only achieve immediate goals, but established a strong foundation for future capabilities.

Why Watch This Webinar?

In this session, you’ll learn:

    • How to eliminate excessive legacy system maintenance costs and integration complexity
    • Planning process and significant benefits of fme’s custom-built archiving tool leveraging Generis CARA and fme’s migration-center
    • An introduction to CARA’s AI-powered capabilities for search and content interaction
    • How the strategic partnership between fme and Generis benefits our clients

Webinar Details

🖥️ Title: Modern Archiving for Life Sciences Enterprises: A Case Study

📅 Date: Recorded Tuesday, October 7, 2025

Who Should Attend?

    • IT Leadership (CIOs, IT Directors, Architects)
    • Regulatory & Quality leaders
    • Records, Information Management and Data Integrity professionals
    • Digital Transformation / Business Systems Owners
    • Migration & Compliance IT teams

If your teams are weighed down by the costs and risks of legacy archiving systems, this is your opportunity to learn how to modernize with confidence, especially if you have implemented or are considering modern solutions within other departments.

👉 View the recording today and be ready to learn efficient and cost-effective archiving with modern solutions.