Pharma web development · Virginia & Maryland

Veeva and HIPAA-ready web development for Virginia & Maryland pharma

Compliant, audit-ready web platforms and Veeva builds for pharma and biotech teams, from Approved Email and CLM to HIPAA-aware patient-facing sites. Built by someone who is actually Veeva certified.

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Veeva Certified (x3) Acquia Certified ABPI Qualified 21 CFR Part 11-aware

Regulated web work punishes generalists

Pharma and biotech web is not ordinary web. Approved Email and CLM run on Veeva. Patient-facing tools need HIPAA. Anything touching records needs audit trails and validation. A general agency learns this on your budget, and on your compliance record.

You need someone who already knows the rules, the tools and the review process, and who will not claim things that are not true, like a Part 11 "certificate" that does not exist.

Veeva, Drupal and HIPAA, done properly

I build and fix regulated web: Veeva CLM and Approved Email, HIPAA-aware sites and portals, and compliant Drupal platforms, designed for validation and audit from the first commit.

For the Mid-Atlantic's pharma corridor

The BioHealth Capital Region and its 350+ life-science firms (AstraZeneca, Novavax and United Therapeutics all have Montgomery County operations) expect regulated-grade digital.
Richmond's Bio+Tech Park and VCU Health, plus the Richmond-Petersburg manufacturing corridor (Phlow, Civica) rebuilding the US essential-drug supply.
Next to the FDA at White Oak: I build audit-trail-ready systems and design for validation, rather than promising a certificate that regulators do not issue.

Real, checkable credentials

Veeva Certified three times over: Vault PromoMats Review and Approval, Approved Email Business, and Approved Email Technical.
Acquia Certified (Drupal) and ABPI Qualified: the platform and the pharma code of practice, in one person.
A decade of regulated delivery, and an eBook, Shipping Software in Pharma, on doing exactly this.

How we work together

Step 1

Compliance-first scope

We map the regulatory surface (Veeva, HIPAA, Part 11) before a line of code.

Step 2

Build for validation

Audit trails, access controls and documentation designed in, not bolted on.

Step 3

Review and approve

Content and change flows that fit your MLR and PromoMats process.

Step 4

Handover you can defend

Documented, validated and audit-ready, not a black box.

You will not be my learning project

I have shipped this work before, certified and in production. We start with a scoped assessment so you see the rigour first. No vague promises, and no invented certifications.

Questions, answered

Are you actually Veeva certified?

Yes, three times: Vault PromoMats Review and Approval, Approved Email Business, and Approved Email Technical.

Is Drupal HIPAA compliant?

Drupal can be built into a HIPAA-aware platform with the right architecture, hosting and controls. Compliance is a function of how it is built and operated, and I build for it.

Do you do Veeva CLM and Approved Email builds?

Yes, both, including the content authoring and the technical setup.

What about 21 CFR Part 11?

There is no Part 11 "certificate"; it is validated per organisation. I design audit-trail-ready, validation-friendly systems so your validation is straightforward.

Where I work

Pharma and biotech teams across Maryland's BioHealth Capital Region, Richmond, Northern Virginia and the wider DC metro, remotely.

Let's talk about your build

A straightforward conversation about your product, your constraints, and how I can help. No sales pitch.