ACCURIDS HUB

Speak every authority's terminology, automatically.

Maintain your established internal data workflows without disruption. ACCURIDS automatically maps your data to the precise terminology required by the FDA, EMA, and NCAs—always current and available via UI or API.

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THE DIFFERENCE

The old way, and the ACCURIDS way.

Adapting Your Existing Systems

You map your terms to each authority's standards by hand, for every submission.

You track shifting controlled vocabularies yourself and redo the work whenever they change.

Every filing is a disconnected, one-off spreadsheet.

IDMP Data Standardization Fabric

Your terms map to every authority automatically.

Mappings stay current as the authorities update their lists.

Reuse it everywhere: in ACCURIDS, via API, or through your AI agents.

How it works

Keep your data as it is. Translate on the way out.

Fast-track compliance with zero forced migrations. Map your data to any authority instantly, while keeping full control of your systems of record.

STEP 01

Keep systems of record untouched.

No forced migrations. Keep your native data formats and update systems like your RIM on your own timeline.

STEP 02

Translate dynamically to any authority.

We map your terms to the exact vocabularies required by the FDA, EMA, and others—automatically kept current.

STEP 03

Pull compliant terms on demand.

Pull authority-ready terms into your dossiers or systems via UI or API. Manual translation drops to zero.

Available Data Assets

Regulatory Data assets available when you need them

Each one is maintained and kept current as the authority updates it.

EMA

European Medicines Agency

SPOR RMSreferentials

SPOR SMSsubstances

SPOR OMSorganisations

SPOR PMSproducts

EMA Article 57authorised products

EMA PMS Publicmedicinal product dictionary

EU ULCMcritical medicines

FDA

Food and Drug Administration

GSRSsubstances

UNIIsubstance identifiers

RxNorm / NDCproduct codes

FEI Numbersestablishment identifiers

National & Regional Authorities

BfArM Productsnational products (DE)

Swissmedic Productsnational products (CH)

ANSM Productsnational products (FR)

NOMA Productsnational products (NO)

Ravimiamet Productsnational products (EE)

Global & Industry Standards

MedDRAmedical terminology

WHODrug KGmedicinal product dictionary

WHO ATCdrug classification

UMLS: ICD-9, ICD-10, ICD-11medical coding

OBO Ontologiesopen biomedical ontologies

More than 250 controlled lists in total, each versioned and kept current as the authorities update them. Selected data assets require a separate subscription at the data provider.

ACCESS

Use the data the way you want.

The same current terminology, available three ways. It stays your data, never locked in.

In ACCURIDS intuitive UI

The same current terminology, available three ways. It stays your data, never locked in.

Integrate with API

Integrate it into your existing systems and workflows.

Let agents draft your dossiers using the correct terms

Let the agents that draft pull it directly.

Built on a Foundation of Unrivaled Expertise

Official Veeva Product Partner

As an official Veeva Product Partner, we guarantee that our platform is designed to work seamlessly with one of the industry's most critical systems.

Veeva Product Partner badge in orange and white.

1st Official IDMP Implementation Partner

Accurids is the only official implementation partner for the IDMP Ontology (Pistoia Alliance), demonstrating unparalleled expertise in setting and applying global data standards.

We Co-Developed the IDMP Ontology

We co-developed the IDMP-Ontology with the Pistoia Alliance, implementing the official ISO Standard.

Supported by IDMP Ontology Sponsors

2 of the leading pharma companies use ACCURIDS

Deployed at leading pharmaceutical companies as the reference data layer in production regulatory and operational workflows.

Frequently asked questions

Can't find your answer?

Our team of experts is dedicated to answering all your questions in detail.

Will using ACCURIDS force us to change the terms in our RIM or migrate our databases?

No, you are entirely in control. ACCURIDS acts as a flexible translation layer, meaning you are never forced to change your source data to achieve compliance. However, if you want to clean up or update the terminology inside your RIM system, ACCURIDS gives you the full capability to do so entirely on your own timeline.

How does ACCURIDS handle changing regulatory standards and outdated terms?

Our built-in data quality engine constantly monitors global authorities like the FDA and EMA. The moment a standard changes, ACCURIDS immediately flags any outdated terms in your pipeline and guides you toward the correct, current terminology—allowing you to make the switch at your own pace without disrupting active workflows.

How does ACCURIDS integrate with Veeva Vault, SAP RIM, and internal authoring systems?

ACCURIDS features a native integration for Veeva Vault to connect your compliance pipelines out of the box. For SAP RIM, internal authoring systems, and broader enterprise data mesh initiatives, our robust native API enables flexible, bidirectional integration. This allows you to seamlessly pull standardized terms into your workflows or sync validated vocabularies back across your entire systems ecosystem.

Can our AI dossier-drafting agents use ACCURIDS?

Yes. Generative AI tools are excellent at drafting text but frequently struggle with strict, exact regulatory vocabularies. ACCURIDS provides a secure, real-time "ground truth" dictionary that your AI agents can query via API, ensuring every automated draft is perfectly compliant from the start.