HAixRev GmbH supports Medical, Marketing and Regulatory teams with the development, review and referencing of scientific content — precise, structured and review-ready.
HAixRev supports pharmaceutical companies in developing, reviewing and referencing medical-scientific content. The focus is on precise claims, robust sources and review-ready materials for internal approval processes.
Supporting every stage of medical content development through expert medical review, scientific writing, evidence-based claim support, and streamlined review workflows—ensuring content is accurate, compliant, and ready for approval.
Scientific review of promotional, non-promotional, and high-level medical congress materials, including abstracts, posters, presentations, claims, visuals, and HCP communications to ensure accuracy, evidence alignment, and regulatory readiness.
Learn more 02Development and refinement of scientifically robust medical content, including HCP materials, patient communications, congress documents, educational resources, and pharmaceutical communications.
Learn more 03Evidence-based claim validation through literature research, reference mapping, source evaluation, and scientific assessment to ensure every statement is supported by credible evidence.
Learn more 04End-to-end Veeva Vault review support including material preparation, claim annotation, reference linking, comment management, version control, and approval workflow coordination.
Learn moreWith a strong foundation in medical-scientific review, evidence evaluation, and pharmaceutical communication, HAixRev supports teams across multiple therapeutic areas. We quickly build indication-specific understanding while maintaining scientific accuracy, reliable source evaluation, and clear, compliant communication throughout the content lifecycle.
Need short-term Medical Review support? Contact HAixRev for project-based support with Medical Review, Medical Writing, referencing or Veeva review processes.