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What makes a successful IDMP submission?

IDMP puts your product data to the test. GVW helps regulatory and data teams turn fragmented product data into trusted, submission-ready information for IDMP and PMS; with clear ownership, governance and the capability to keep that data accurate as products change and EMA requirements evolve.

Check Your PMS Readiness

PMS Enrichment Deadlines

September 2026: eAF Mandatory for CAP Variations

Workstream

2025

2026

2027

XEVMPD — pack size enrichment

Non-critical medicines*

PMS enrichment: structured pack size info

ULCM*

Non-critical medicines*

PMS enrichment: manufacturer & MBO data

ULCM*

Non-critical medicines

Extended deadlines = *

Time left to get PMS-ready

The clock is already running

00 days
00 hours
00 minutes
00 seconds

Sound familiar

Most regulatory teams are working toward IDMP with the same four obstacles.

These are the gaps we see most often when we start a PMS or IDMP readiness engagement, not because teams lack effort, but because the data and processes were never built for this level of structure.

Limited awareness of IDMP and the linked EMA initiatives ePI, ESMP, SPOR and how they connect to day-to-day submissions.
Data management and data governance practices that aren’t yet embedded as a habit, only a project.
Enterprise-wide data fragmentation caused by disconnected Regulatory, Quality, and Supply Chain systems
A technology landscape that wasn’t built for IDMP-level interoperability.

★

Why Global Value Web

Six phases, one trusted product data foundation

Executing for today, organizing for tomorrow, a structured, standards-based approach aligned with EMA PMS guidance, ISO IDMP standards and industry practice.

Strategic planning

A clear IDMP vision and roadmap aligned with your regulatory and business priorities, not a generic template.

Regulatory business process consulting

Future processes, operating models and governance structures designed for how IDMP actually needs to run.

System implementation & integration

Assessing and designing the technology architecture your data needs to move through, not around.

Data analysis, acquisition & management

Quantifying the real remediation effort, then applying a pragmatic, prioritised approach to fixing it.

Data transfer

Moving product data from xEVMPD, SIAMED and legacy sources into PMS without losing what already works.

Transition to IDMP & maintenance

Because compliance doesn't end at go-live — it has to keep working every time your product data changes.

“

We help you build the trusted product data foundation that makes IDMP, PMS and whatever EMA asks for next, achievable.

Global Value Web Regulatory & data consulting

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Our people love your data

What makes a successful IDMP submission?

PMS Enrichment Deadlines

Time left to get PMS-ready

Most regulatory teams are working toward IDMP with the same four obstacles.

Why Global Value Web

Six phases, one trusted product data foundation

Strategic planning

Regulatory business process consulting

System implementation & integration

Data analysis, acquisition & management

Data transfer

Transition to IDMP & maintenance

Speak with Our Experts Now!

Case Studies

LIMS Master Data Configuration for Leading API Manufacturer

Read More

LIMS-Master Data Maintenance for Big Pharma client

Read More

Saving stability testing efforts for a fortune 20 company

Read More

Featured Insights

Unifying An Enterprise Through Master Data

Read More

Data As A Backbone For Operational Excellence

Read More

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