Pharmaceutical software systems

Made in Europe. Designed for global pharma markets.

Pharmaceutical software from R&D to market

Connected, GxP-ready systems for regulated pharmaceutical teams — built on 20+ years of pharma software experience.

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20+ years in pharmaceutical software

GxP & validation support

AI-assisted workflows

Flexible deployment & licensing

Start with your business need

Start with the problem you want to solve

You do not need to know the nData product names. Explore solutions by pharmaceutical process, the operational problem you want to address and the outcome your teams need.

Explore solutions by business need

Explore the nData product suite

Focused applications for specific pharmaceutical processes, available independently or as part of the connected ecosystem.

ePM

Project & Portfolio

Portfolio and project management layer connecting R&D strategy, execution, resources, budgets, risks and stage-gate decisions.

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eRA

Regulatory

Regulatory management platform for registrations, submissions, variations, renewals, authority communication and readiness.

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eQCP

Quality Control

Quality control planning platform connecting QC master data, samples, test orders, laboratory resources, scheduling, results and deviations.

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eAW

Artwork & Packaging

Artwork management platform for mockups, versions, approvals, change requests, required documents and lifecycle control.

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eDOCS

Documentation

Controlled document management platform for SOPs, work instructions, policies, forms, records, workflows and audit-ready evidence.

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eTMF

Clinical Operations

Electronic Trial Master File platform for study documentation, TMF structure, completeness, reconciliation, inspection readiness and audit evidence.

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eGO

Launch Management

Launch management platform for country readiness, cross-functional activities, milestones, dependencies and market launch evidence.

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eLAB

R&D Laboratory

R&D laboratory platform for experiments, laboratory diaries, samples, structured results and product-to-reference comparison.

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eTRANSFER

Technology Transfer

Transfer project platform for portfolio care changes such as production site changes, MAH changes, ownership transfers, readiness gates, risks and evidence.

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Explore all products

Specialized products. One connected ecosystem.

Cover the journey from the initial product idea through development, registration and launch to ongoing portfolio care.

Focused adoption

Use each product independently

Start with the process that needs improvement without replacing the rest of your system landscape.

Connected adoption

Connect products into one continuous process

Share product, market, project and workflow context so downstream teams can continue from controlled upstream information.

Idea & portfolio

Evaluate opportunities, prioritize investment and define what moves into development.

ePM

Development & evidence

Coordinate R&D work and preserve laboratory and clinical development evidence.

ePM eLAB eTMF

Registration

Plan submissions, registrations, commitments and market-specific requirements.

eRA

Transfer & readiness

Coordinate technology transfer, quality activities and operational readiness.

eTRANSFER eQCP

Market launch

Align country readiness, approved artwork, documents and launch dependencies.

eGO eAW eDOCS

Portfolio care

Manage renewals, variations, product changes and ongoing controlled evidence.

eRA eTRANSFER eAW eDOCS

Connected context follows the product.

When systems are integrated, regulatory teams can build on what is being developed, launch teams can follow what is being registered, and artwork teams can act on the relevant market and regulatory requirements. Documents, evidence and status remain connected instead of being reconstructed between departments.

Experience in practice

Evidence from real pharmaceutical operations

Selected customer relationships and examples of nData systems supporting day-to-day pharmaceutical work.

Selected customers

A selection of pharmaceutical and life-science organizations we have worked with.

Case studies

Examples of nData systems supporting real pharmaceutical operations.

Quality control operations

Faster, more effective release-testing planning with eQCP

Problem: Hundreds of batches were awaiting release testing. Laboratory capacity was not fully utilized, while planning was inefficient and time-consuming.
Solution: The customer introduced eQCP to coordinate test planning, laboratory capacity and operational changes in one structured workflow.
Result: Planning is now faster and more effective. Unexpected events, such as instrument or analyst unavailability, can be addressed within minutes instead of hours or days.

View eQCP Project and portfolio management

Clear portfolio control across thousands of projects with ePM

Problem: The customer manages thousands of projects, including hundreds of active initiatives. Work was coordinated through Microsoft Project and Excel files, making it difficult to identify the current status, determine which file was authoritative and maintain consistent oversight.
Solution: The customer introduced ePM as the central system for project and portfolio data, replacing fragmented files with a shared, structured source of information.
Result: Four project managers now manage the full portfolio with a clear view across projects. The system continuously monitors project data and automatically identifies potential problems.

View ePM Artwork and packaging operations

Controlled artwork lifecycles without a dedicated department

Problem: Managing the complete artwork lifecycle was demanding for a smaller pharmaceutical organization without a dedicated artwork department.
Solution: The customer introduced eAW to connect the required roles and activities automatically within a defined, controlled workflow.
Result: Artwork lifecycles are now initiated and managed automatically from registration requirements held in eRA. The customer retains control of the process with minimal manual effort and greater confidence that artworks will be ready when required.

View eAW

From software to a working solution

nData supports customers from solution design through implementation, rollout and long-term operation.

Process & solution design

Translate regulated workflows, roles and data into a practical product setup.

Implementation & configuration

Configure modules, workflows, permissions and templates around the operating model.

Data migration & integration

Prepare legacy records and connect the product with the surrounding system landscape.

Validation, training & support

Support validation evidence, rollout, adoption and controlled product evolution.

Explore implementation services

About nData

Meet the people behind the products

Get to know the team combining pharmaceutical process experience with product development, implementation and long-term customer support.

More about nData

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Let's discuss what you need to improve.

Talk directly to people who understand both the software and the pharmaceutical processes behind it — whether you are evaluating a product, improving a process, replacing a legacy system or planning a broader digitalization initiative.