iFeed is a regulated-healthcare intelligence, platform and services company working across bioanalytical, bioequivalence, clinical trials and quality.
iFeed supports organisations working in bioanalytical, bioequivalence, clinical trials and quality. These are the areas where data integrity and quality management decide whether a submission holds up to inspection. We work in three ways: regulatory intelligence that tracks change across the FDA, EMA, MHRA, ICH and the EDQM; delivery services that place experienced people alongside your team; and ClinAssure, a controlled workspace in development for readiness, evidence and delivery.
The approach is deliberately narrow: four domains, connected through one readiness view rather than four disconnected conversations.
Eight years across CRO and sponsor environments in bioanalytical, bioequivalence and clinical trials, focused on operations, quality and execution. BPharm; M.S. Pharm (NIPER).
LinkedIn ↗Operations, quality and execution support across bioanalytical, bioequivalence, clinical trials and quality, as a project or an extension of your team.
ClinAssure is our controlled workspace in development, designed to connect QMS, document control, training, evidence, submission readiness and audit readiness so teams can move from scattered work to clear, inspectable deliverables.