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MLR-ready formatting for Veeva Vault PromoMats

Veeva Vault PromoMats Content Formatting

Pubrica’s Veeva Vault PromoMats content formatting service supports pharma and medtech marketing operations teams, MLR coordinators, agencies and regulatory affairs teams by reformatting promotional assets to the client’s PromoMats document structure, with reference annotation, citation tagging, metadata population and a formatting QA check against the MLR submission checklist, in line with FDA OPDP / eCTD submission standards. Our medical writers and content strategists carry out the work in-house; a named subject specialist leads your project from brief to delivery, and a second, independent reviewer checks each asset before it reaches you.

  • Asset reformatted to the client's PromoMats document structure requirements — included in every engagement
  • Reference annotation and citation tagging within the document — included in every engagement
  • Metadata field population — included in every engagement
  • Prepared to named standards, including FDA OPDP / eCTD submission standards
  • A published starting price: $150 per standard asset
Included in Scope Not Included

Asset reformatted to the client's PromoMats document structure requirementsIncluded

Reference annotation and citation tagging within the documentIncluded

Metadata field populationIncluded

Formatting QA check against the client's MLR submission checklistIncluded

Work outside the agreed scopeNot included

Brief → scoping → draft → delivered

Included in every project
  • Asset reformatted to the client's PromoMats document structure requirements
  • Reference annotation and citation tagging within the document
  • Metadata field population
  • Formatting QA check against the client's MLR submission checklist
  • Delivery of the asset ready for direct upload into the client's Vault PromoMats workflow
$150Published starting price
5–10 business daysFrom brief to final delivery
5 deliverablesItemised on this page
ISO 9001:2015Quality management certified · cert. H3CR9TCU20251212INDQM10N

Deliverables

Veeva Vault PromoMats Content Formatting Deliverables

Each deliverable below is prepared in-house by Pubrica’s medical writers, video producers and content strategists.

Asset reformatted to the client's PromoMats document structure requirements Asset reformatted to the client's PromoMats document structure requirements.
Reference annotation and citation tagging within the document Reference annotation and citation tagging within the document.
Metadata field population Metadata field population (claim tags, content module identifiers, reuse/similarity flags where applicable).
Formatting QA check against the client's MLR submission checklist Formatting QA check against the client's MLR submission checklist.
Delivery of the asset ready for direct upload into the client's Vault PromoMats workflow Delivery of the asset ready for direct upload into the client's Vault PromoMats workflow.

Who We Serve

Organisations We Support with Veeva PromoMats Content Formatting

We format PromoMats assets for teams that manage, produce or submit promotional materials.

Pharma and medtech marketing operations teams managing high volumes of promotional assets through Veeva VaultThey use this service to keep high asset volumes moving through review.
In-house MLR coordinators who need external formatting support to keep review queues movingThey use this service to keep high asset volumes moving through review.
AgenciesThey produce content for pharma clients and must deliver PromoMats-ready files rather than raw creative.
Regulatory affairs teamsThey prepare submission-track promotional materials that require eCTD-compliant structure.

Compliance and Standards

Compliance Standards for Veeva PromoMats Content Formatting

The submission standards and review workflows that PromoMats formatting must support.

FOES

FDA OPDP / eCTD submission standards

PromoMats-formatted content for submission-track materials must conform to eCTD-compliant structure; correctly tagged metadata and annotated references are what let the platform auto-generate submission-ready packages.

MLR

Internal MLR (Medical, Legal, Regulatory) review workflows

Metadata tagging (claim references, content module IDs, reuse status) determines which MLR review tier an asset is routed to, directly affecting review turnaround.

ISO9001:2015

Quality management (cert. H3CR9TCU20251212INDQM10N)

Pubrica’s certified quality management system governs how each project is run, reviewed and documented.

Responsible Use of AI

Our Approach to AI Use in Veeva PromoMats Content Formatting

We use generative AI tools only for drafting and iteration, and never where the output could be mistaken for verified clinical data or a real patient.

How We Use AI ToolsWe use AI tools for layout variations, colour systems and first-pass drafts, which a specialist then corrects against the brief and the applicable brand or clinical standards.
Where We Do Not Use AIWe do not use AI to generate any image, figure or quote presented as real clinical data, a real patient or a verified result, and no material is released without a named reviewer’s sign-off.
Your AI Use DeclarationYour declaration states the tool used, the stage at which it was used and the human oversight applied, because MLR/PRC reviewers, funders and regulators increasingly expect this to be stated.

Why We Do Not Publish AI Accuracy Figures

Accuracy figures for AI design and content tools are usually reported by the vendors that sell them.

For this reason, we do not quote an accuracy figure of our own. We tell you which tool was used on your project, at which stage, and what the named reviewer changed afterwards.

Our Process

How a PromoMats Formatting Project Works

Each project follows four steps, with a draft review before final production so that any misunderstanding of the brief is corrected early.

Step one

Submit Your Brief and Reference Material

Tell us which assets need formatting, who will review them and anything that must or must not appear, and send your PromoMats document structure requirements, MLR submission checklist and source material.

Step two

Scoping Consultation

We confirm the audience and the applicable standards and, for scoped projects, the factors that determine the final quote.

Step three

Concept and First Draft

A subject specialist and the production team prepare the first version against the brief, and it is reviewed internally for accuracy before it is sent to you.

Step four

Revisions and Final Delivery

We incorporate your revisions and deliver the files listed on this page, including the working files, so the material can be updated later without starting again.

Request a Free Scoping Assessment for Your PromoMats Content

We confirm the cost, timeline and applicable standards before you commit. The assessment is free and takes two business days.

What We Need From You
The briefThe purpose of the material and its intended audience
Reference materialExisting assets, brand or style guidelines, prior approved versions
The audienceClinician, patient, payer, investor or internal team
ConstraintsAnything that must or must not appear, and the standards that apply
The deadlineYour deadline, including any congress or submission window
Approval routeWho approves the work, and whether MLR/PRC review is involved

Our Experts

Your PromoMats Content Team

The same named team of specialists works on your project from scoping to delivery.

Subject expertA subject matter expert matched to your topic

Determines what the work can claim on the basis of the evidence, and advises you clearly when the brief asks for something the evidence does not support.

OwnsScope, judgement, interpretation
Reviews againstThe applicable standards for this work
FieldMatched to your topic
Dr. DivyaPhD in Life Science · second reviewer

Reviews the work independently of the first pass, with particular attention to factual accuracy. Any disagreements are logged and adjudicated by a third reviewer.

OwnsIndependent second review
Reviews againstThe applicable checklist
Adjudicated byA third reviewer
Dr. AntonyProduction and delivery lead

Responsible for file formats, compliance with the destination’s specification and the handover of working files, so that the delivered files match your brief.

OwnsProduction and delivery
Reviews againstThe destination's own specification
Second-checked byA second production reviewer
Mr. JohnCompliance and standards reviewer

Checks that each deliverable meets the standards that apply to it, such as MLR requirements, WCAG or the relevant regulatory guidance.

OwnsStandards and compliance review
Reviews againstThe standards listed on this page
ToolsThe current published guidance for each

Evidence Base

Why Veeva PromoMats Content Formatting Matters

Content formatted to the PromoMats document structure supports efficient MLR review in the following ways.

01 Reused, pre-approved content needs less review depthAssets built from reused, pre-approved modules typically need less review depth than wholly new material.
02 Consistent structure reduces review roundsAssets that follow the required document structure spend fewer review rounds on formatting corrections.
03 Annotated references support faster checkingReferences annotated and linked at submission reduce manual checking and the delays caused by annotation errors.
04 Review time goes on content, not formattingAssets that arrive formatted to the PromoMats document structure, with references annotated, spend their review time on content rather than on formatting corrections.

Packages

Veeva PromoMats Content Formatting Pricing

A published starting price for the standard scope, with larger projects quoted before work begins.

Standard

Veeva Vault PromoMats Content Formatting

Per asset, covering formatting of a single promotional or medical content piece to PromoMats specification (document structure, reference annotation, metadata/claim tagging) ready for submission into a client's MLR review workflow; complex multi-component assets (e.g., interactive or multi-channel pieces) are quoted separately.

$150Published starting price

Delivery 5–10 business days

  • ✓Asset reformatted to the client's PromoMats document structure requirements
  • ✓Reference annotation and citation tagging within the document
  • ✓Metadata field population (claim tags, content module identifiers, reuse/similarity flags where applicable)
  • ✓Formatting QA check against the client's MLR submission checklist
  • ✓Delivery of the asset ready for direct upload into the client's Vault PromoMats workflow
Get a free quote

Quality Assurance

Our Service Commitments

Our revision commitment, its limits and the remedy are set out before work begins.

Our revision commitment

Free Revisions Against the Agreed Brief and Named Standards

Within the agreed scope, we revise at no additional cost any work that does not match the brief or a standard named on this page.

01

The brief is confirmed before production

We confirm the brief at scoping so that any misunderstanding is resolved before production starts.

02

A named reviewer approves the work before delivery

The review is carried out against the standards listed on this page.

03

AI use is disclosed

We tell you which tool was used, at which stage, and what the reviewer changed afterwards.

04

Working files are handed over

You receive the working files, so the material can be updated later without starting again.

Client Testimonials

“The content cleared MLR on the first pass, which almost never happens with an outside writer.”
HowardMedical affairs lead, pharmaceutical company

USA

Veeva Vault PromoMats Content Formatting FAQs

Frequently Asked Questions About Veeva PromoMats Content Formatting

If your question is not answered here, please ask an expert. No quote is required.

Pubrica’s Veeva Vault PromoMats content formatting service supports pharma and medtech marketing operations teams, MLR coordinators, agencies and regulatory affairs teams by reformatting promotional assets to the client’s PromoMats document structure, with reference annotation, citation tagging, metadata population and a formatting QA check against the MLR submission checklist, in line with FDA OPDP / eCTD submission standards. Our medical writers and content strategists carry out the work in-house; a named subject specialist leads your project from brief to delivery, and a second, independent reviewer checks each asset before it reaches you.

The core deliverable is each asset reformatted to your PromoMats document structure requirements. The full list appears on this page under Deliverables.

Assets built from reused, pre-approved modules typically need less review depth than wholly new material.

Our specialists apply these published findings and the relevant regulatory guidance when planning and reviewing each project.

The published starting price is $150 per asset, covering formatting of a single promotional or medical content piece to PromoMats specification (document structure, reference annotation, metadata/claim tagging), ready for submission into your MLR review workflow. Complex multi-component assets (e.g., interactive or multi-channel pieces) are quoted separately before work begins.

Pharma and medtech marketing operations teams managing high volumes of promotional assets through Veeva Vault

In-house MLR coordinators who need external formatting support to keep review queues moving

PromoMats-formatted content for submission-track materials must conform to eCTD-compliant structure; correctly tagged metadata and annotated references are what let the platform auto-generate submission-ready packages.

Our specialists apply this standard from the start of the project rather than correcting for it after review.

Request a Free Scoping Assessment for Your PromoMats Content

We confirm the cost, timeline and applicable standards before you commit. The assessment is free and takes two business days.

Get a free quote

Regulations

Check your project against this rule

  1. 1Your work
  2. 2Your details
  3. 3Send
What do you need?

Material you send is held under signed confidentiality, with access limited to the assigned team and encrypted transfer. It is not used to train anything and is not passed to third-party tools. Ask for the agreement before you send anything you would rather cover first.