Do you have experience with FDA and EMA regulatory requirements for pharma websites?

Yes. We build pharmaceutical digital platforms with regulatory compliance as a baseline requirement, not an afterthought. Our process includes a regulatory brief at project start to ensure content architecture and user flows are designed around your MLR review process from day one.

Can you build HCP portals with gated content for healthcare professionals?

Absolutely. We design and develop HCP portals, prescriber tools, and medical affairs platforms with appropriate access controls and content governance built in. We have built multi-market platforms each with their own content approval chain and localization requirements.

Which CMS platforms do you implement for pharmaceutical companies?

We implement Adobe AEM, Magnolia, Drupal, and Sitecore for pharmaceutical digital teams. Each is configured with granular editorial permissions so content teams can publish without creating compliance exposure, and we integrate with existing MLR workflow systems where needed.

Digital Solutions for Pharmaceuticals

Regulatory-Aware Development from Day One

The pharmaceutical industry operates under a level of scrutiny that most digital agencies simply are not equipped to handle. Regulatory frameworks — FDA, EMA, ANVISA, local health authorities — impose strict requirements on how products, indications, and clinical data are presented online. PixelEruption designs and develops digital platforms that are built to meet these requirements from the first line of code, not patched to comply after the fact.

HCP Portals, MLR-Aligned Architecture, and Multi-Market Delivery

We build HCP portals, prescriber tools, product information sites, medical affairs platforms, and corporate communications hubs. Every project starts with a regulatory brief so that content architecture, data handling, and user flows are designed around your MLR review process — not retrofitted to survive it. We have built platforms for brands operating across multiple markets simultaneously, each with its own content approval chain and localization requirements.

Scientific Precision in Digital Detailing and Medical Communications

From animated molecule visualizations and digital detailing tools to responsive email campaigns for medical congresses, our team delivers work grounded in scientific precision. We know what a PI page needs to include, how safety information must be surfaced, and how to balance medical accuracy with the visual quality your brand deserves.

Implementation Benchmarks: What to Plan For

A mid-size pharmaceutical multi-market CMS implementation typically spans 12–24 months from brief to go-live, depending on platform and market count. MLR workflow configuration takes 6–10 weeks on AEM (with a reference implementation base) and 10–14 weeks on Sitecore XM Cloud. Content approval cycles drop from an industry baseline of 10–14 days to 3–5 days after a mature MLR workflow is in place. Our pharma implementations cover compliance frameworks across FDA 21 CFR Part 11, EMA, and ANVISA simultaneously, with market-specific content governance for 5–20 markets on a single platform.

Direct Access: No Account Manager Between Your Brief and the Build

What makes PixelEruption different from a larger pharma-specialized agency is direct access. You talk to the developer and designer who are actually building your platform — not an account manager who passes your compliance requirements down a chain. That means fewer distorted briefs, faster iteration cycles, and no version of your regulatory requirements getting lost in translation between floors.

What We Deliver

Pharmaceutical Web Development AEM Development CMS Development & Content Entry Pharmaceutical SEO Web Design & Development Email Marketing Graphic Design Animated Banners

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Frequently Asked Questions

Do you have experience with FDA and EMA regulatory requirements for pharma websites?: Yes. We build pharmaceutical digital platforms with regulatory compliance as a baseline requirement, not an afterthought. Our process includes a regulatory brief at project start to ensure content architecture and user flows are designed around your MLR review process from day one.
Can you build HCP portals with gated content for healthcare professionals?: Absolutely. We design and develop HCP portals, prescriber tools, and medical affairs platforms with appropriate access controls and content governance built in. We have built multi-market platforms each with their own content approval chain and localization requirements.
Which CMS platforms do you implement for pharmaceutical companies?: We implement Adobe AEM, Magnolia, Drupal, and Sitecore for pharmaceutical digital teams. Each is configured with granular editorial permissions so content teams can publish without creating compliance exposure, and we integrate with existing MLR workflow systems where needed.

Contact Us

At PixelEruption, we believe strong partnerships begin with clear communication. Whether you’re a global enterprise or an innovative institution, our team is ready to listen, collaborate, and design digital solutions that meet your most ambitious goals.

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