FATHOM / Industries / Pharmaceutical & Life Sciences
Pharma web platforms operate under constraints most agencies never meet: regulatory review on every sentence, market-specific content, and audiences split between HCPs and the public. We build the infrastructure that makes those constraints workable — approval-gated editorial workflows, multi-market content federation, and self-hosted data.
01
Editorial workflows where nothing goes live without the required sign-off chain — regulatory review built into the CMS, not a promise in an email.
02
One system serving GCC market variants with market-specific approvals — shared where allowed, separated where required.
03
Company, pipeline, and responsibility content structured for investors, partners, and regulators — bilingual as standard.
Enterprise platform track
from AED 35,000
Multi-market federation
+ AED 19,500
Additional language (engineering)
+ AED 2,750 / language
All anchors come from the public Scope Estimator on our homepage — configure your exact scope there and the math stays the same.
Your regulatory affairs team — always. Our contribution is structural: workflows that make skipping the approval step technically impossible, and audit trails showing who approved what, when.
Yes — gated sections with declared-audience access are a standard pattern we implement, with your legal team defining the gate's strictness.
Book a strategic architecture call — or run the estimator and send us your pre-filled scope.