Pharma Software Development

Early research produces large volumes of experimental, compound and assay data, often scattered across instruments, notebooks and shared drives. We build experiment tracking and compound registration tools, connect electronic lab notebooks and analysis software through APIs, and add scientific search across internal reports and published literature, so researchers can find earlier results quickly and decide what to test next using complete, well-labelled data.

Sponsors, CROs and sites all touch trial data, and every change has to be attributable to a person and a reason. We build study setup tools and site portals, electronic data capture forms, patient-reported outcome and eConsent apps, and monitoring dashboards that flag missing or inconsistent data early. Integrations with randomisation, safety and trial management systems keep records consistent, with a full audit trail on every entry, correction and signature.

On the shop floor, paper batch records and disconnected equipment logs slow down batch release and make deviations harder to investigate. We build electronic batch records, equipment and cleaning logs, and tablet apps that guide operators through each step, capture data at source and connect to your MES, ERP and quality systems. Review by exception then lets QA focus on the entries that genuinely need a closer look.

Quality teams manage deviations, CAPAs, change controls, training and controlled documents, often across several tools that do not talk to each other. We build workflows with electronic signatures, role-based approvals and full history, link quality events to the batches and documents they affect, and support regulatory teams with submission tracking and document assembly, all structured around how auditors and inspectors actually examine records.

Medicines have to be traceable from production line to patient, often through temperature-controlled routes and several partners. We build inventory and distribution tools, bring cold-chain sensor and data logger readings into one place with alerting, and exchange serialisation and shipment data with packaging lines, wholesalers and logistics providers through EDI and APIs, so every pack can be located and every temperature excursion investigated with the facts at hand.

Field teams, medical science liaisons and medical information services need accurate content and properly recorded interactions. We build CRM extensions and field apps for planning visits and logging conversations, medical information tools that handle enquiries and route possible adverse events to the safety team, and content workflows with review and approval steps, so materials are checked before use and every interaction can be traced later.