Integrated Regulatory Information Management System

for Pharma Biotech

In today’s complex life sciences landscape, regulatory affairs and operations require more than manual tracking or spreadsheets, they demand intelligent automation, visibility, and compliance control.

DDi’s Integrated Regulatory Information Management System (RIMS) is built for pharma and biotech companies to unify global regulatory processes, automate workflows, and enable informed decision-making across the entire product lifecycle.

Our regulatory information management software helps your organization eliminate silos, reduce compliance risks, and accelerate submission readiness, all from a single, secure platform.

Why Choose DDi’s Regulatory Information Management Software?

Visu is designed not just to manage information, but to automate and transform how your teams collaborate and comply. Here’s how DDi’s platform drives regulatory excellence:

Automation at Every Step – Streamline submission tracking, dossier preparation, and document versioning through automated workflows that reduce manual effort and turnaround time.
Global Compliance Management – Track global regulatory submissions in real time and maintain up-to-date records aligned with regional requirements.
Centralized Collaboration – Provide a single, unified view of all regulatory activities, ensuring teams, affiliates, and partners work from the same trusted data source.
Smart Analytics & Insights – Access powerful dashboards and reporting tools to support faster, more informed decisions.
Audit-Ready Documentation – Maintain transparency and traceability with an always-compliant, inspection-ready repository.

Transforming Regulatory Operations with a Connected Platform

Our regulatory operations platform integrates seamlessly with your existing systems, bringing together data, processes, and documents under one digital framework.

With DDi’s RIMS, your organization can:

Simplify global submission management and publishing.
Track product registration and lifecycle milestones.
Gain end-to-end visibility into regulatory status across geographies.
Reduce compliance risks through proactive monitoring and alerts.
Enable faster market access by improving regulatory readiness.

Whether your goal is to modernize regulatory operations or achieve global harmonization, DDi’s regulatory information management system offers the flexibility and intelligence you need to stay ahead.

Tailored to Your Business Needs

Every organization has unique processes, that’s why DDi delivers customized RIM solutions that fit your operational goals, scale, and budget.

From small biotechs to global pharmaceutical enterprises, our regulatory operations software can be configured to match your business model while ensuring alignment with compliance requirements.

Custom module integration
Configurable workflows
Cloud or hybrid deployment options
Secure, validated environment

Our expert team ensures a smooth implementation and continuous optimization so your regulatory teams can focus on what matters most, bringing safe, compliant products to patients faster.

Why DDi? Your Partner in Regulatory Digital Transformation

DDi has been empowering global life sciences companies with intelligent automation, data-driven solutions, and deep regulatory expertise. Our regulatory information management software is backed by years of experience in compliance, technology, and process transformation.

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