CODE GxP is a pharmaceutical digital agency working with pharma, biotech, medtech and life sciences companies across Europe. We cover pharmaceutical web design, website development, HCP portals, multilingual rollouts and the pharmaceutical SEO and content that makes them findable.
We design, build and grow pharmaceutical websites and digital platforms for regulated companies: corporate pharma sites, HCP portals, product catalogues, multilingual pharmaceutical websites, accessibility work and the pharma SEO and content that makes them findable.
CODE GxP builds corporate websites and digital platforms for pharmaceutical and regulated companies across Europe.
A pharmaceutical laboratory with a regulated product portfolio, a CDMO selling manufacturing capacity and a biotech raising a funding round need completely different websites. Our pharmaceutical web design work starts from how your segment actually buys.
Entry points by discipline and by sector, for teams that already know what they are looking for.
The questions that come up in almost every first conversation about a pharmaceutical web project.
Yes, in most cases. The EAA has applied since 28 June 2025 to companies with more than 10 employees and over EUR 2 million in turnover that serve consumers in the EU. The reference standard is EN 301 549, which points to WCAG 2.1 AA. Existing content has until 28 June 2030. Patient-facing pharma sites, e-commerce and booking flows are squarely in scope.
We build to your compliance process rather than claiming a certification that does not exist. There is no such thing as an “EMA compliant website” — the EMA regulates medicines, not agency deliverables. What we do is structure content so medical, regulatory and legal review is built into the workflow, separate public and professional access properly, and keep an audit trail of what was approved.
Yes. We work with pharmaceutical, biotech and life sciences companies across Europe, delivering in English as standard. Several of our projects are multilingual rollouts covering up to seven languages at once, and we have handled domain migrations that preserved country-level SEO continuity throughout, so rankings and traffic carried over rather than resetting after launch.
Yes. We migrate from any platform, working either from the database or through structured scraping when database access is not available. The part that matters is not the export — it is preserving URLs, permissions and search visibility. We have migrated a 1,550-document library with inherited permissions and legacy URLs intact.
A corporate pharma site typically runs three to six months from kick-off to go-live. The variable is rarely development — it is how long medical and regulatory review takes on your side, and how much of the product data has to be restructured before it can be published.
Both. Alongside web and platform work we run SEO, content, LinkedIn and social media management, paid media and brand work for regulated companies. Social media for pharma is a specific discipline — adverse-event monitoring and approval workflows are part of the service, not an afterthought.
Corporate pharmaceutical websites, HCP portals, product catalogues or a migration off a legacy platform. Tell us the context and the scope you have in mind and we will tell you how we would approach it.