Private AI for Business

Nigeria / NAFDAC / product registration

NAFDAC registration is a dossier and timeline problem, not one upload.

We build private workflows that organize registration and renewal dossiers, evidence, compliance responses, and official timelines for NAFDAC product applications. The workflow prepares the pack; NAFDAC decides registration after its evaluation.

Dossier mapTimeline trackerCompliance responsesRenewal calendar
A neutral example of the same workflow pattern, run on supplied synthetic material.

Pattern demonstration / same workflow, synthetic material

Fixed-scope setupClient-owned accountsDraft-and-review firstFull handover

The work behind a NAFDAC file

The product file is long and versioned.

Food, drug, and product applications repeat the same assembly problem: keeping formulations, labels, test reports, and correspondence aligned.

01 / DOSSIER

Map the product file

Organize the current registration or renewal file, versions, submissions, and official correspondence for one product.

02 / TIMELINE

Track the official clock

Place acceptance, evaluation, compliance response, and renewal dates on the product calendar with the official working-day frame.

03 / RESPOND

Prepare the response

Assemble the requested documents, evidence, and open questions for a NAFDAC compliance directive or variation.

The registration boundary

The system prepares the dossier. It cannot register the product.

NAFDAC

Approval stays with NAFDAC

The workflow prepares and tracks evidence. Evaluation, approval, certificate, and conditions remain with NAFDAC.

TECHNICAL

Qualified reviewers own content

Formulation, safety, efficacy, labeling, and technical responses stay with the applicant's qualified professionals.

CURRENT

Confirm portal and fees

The current NAFDAC portal, forms, fees, and working-day periods are confirmed against official guidance before a build.

A first registration workflow

Pick one product and one official stage.

Choose the product

Select the food, drug, or regulated product file that the company needs to register or renew.

Map the dossier

List the forms, technical documents, labels, test reports, and evidence required by the current official guidelines.

Track the timeline

Record acceptance, response, evaluation, and certificate dates using the official working-day guidance for the product type.

Build the response pack

Prepare the requested documents, source index, and open questions for the technical owner and submission route.

A registration file is easier to move when every official question has a document behind it.

Why trust Pristine3D?

We build and operate production software.

Pristine3D Ltd builds and operates live digital products, and we run private AI workflows internally as part of our own operations. We scope around your real workflow: the documents you own, the questions your team asks, and the access boundary you approve. Based in Lagos, Nigeria, we work remotely with clients worldwide.

METHOD

We start with the actual workflow

One input, one output, one test set, and one person who owns the result. We scope a real workflow instead of a transformation programme.

OWNERSHIP

The boundary stays visible

Cloud, model, storage, and messaging accounts stay in your name. The chosen data path, access rules, test record, documentation, and training are part of the agreed scope.

Pricing / fixed scope

Know the starting numbers before you ask.

The final quote follows the workflow. Infrastructure and model bills stay on your accounts.

Annual support

Starting from
$3,000 / ₦1.5m
per year

Standard care for one delivered workflow. Optional. Larger deployments and active monitoring are separately scoped.

See support

Architecture review from $500. Standard annual support is $3,000 / ₦1.5m per year for one delivered workflow. New workflows, integrations, active monitoring, and infrastructure are separately scoped; infrastructure, model, storage, and messaging bills stay on client accounts. Full pricing and what changes the quote

Straight answers

Common questions.

Does this guarantee NAFDAC registration?

No. It organizes and tracks the dossier. Evaluation, approval, certificate, and conditions remain with NAFDAC.

Can it submit through NAPAMS?

It can prepare portal inputs and evidence. Submission, credentials, and official communication stay with the applicant and its authorized staff.

What timelines does this use?

The official guideline period for food is 90 working days and for drugs is 240 working days after acceptance, with variations for minor changes; the current official version is confirmed before use.

Own your knowledge base

The model is not the product. The knowledge base is.

Documents, the retrieval index, access rules, and the workflows built around them are the asset, and they compound. We deploy so the knowledge base stays yours: on your accounts, in the environment you choose, under access rules your team defines. The model behind the answers is a connector, so the knowledge base moves with you, not with a vendor.

THE ASSET

Your corpus, your index

The document store, metadata, and retrieval setup live on accounts you own. No vendor holds the corpus.

THE LOCK-IN

Models are swappable parts

Change the model provider, move regions, or go local without rebuilding the knowledge base or the workflow.

THE ALPHA

The knowledge base is the alpha

Every improvement to the corpus improves the answers, and the improvement stays with you, not with a vendor.

Keep exploring

Related setups.

Start with the product file

Which registration or renewal is moving slowly?

Tell us the product, the official stage, the dossier you hold, and the technical owner. We will scope a workflow around the current NAFDAC requirement.

Prefer email? Message us at hey@pristine3d.com.