Services

Aureole empowers your projects with seamless, end-to-end solutions, offering tailored medical writing, scientific review, data quality checks, and other clinical research services — all underpinned by expertise across multiple domains and delivered with unmatched precision and timeliness to support every phase of your clinical and research endeavors.

Preclinical and Translational Research

Pharmacology (ADME, PK/PD) and toxicity reports
Safety reports
Nonclinical summaries

Publication Writing & Scientific Communication

Abstracts, manuscripts, posters, oral presentations, review articles, white papers
Publication planning, congress planning
Scientific narrative, lexicon, and communication platforms
Publication extenders: plain language summaries, graphical abstracts, infographics, audio/video content
Medico-legal reviews (MLR), Medical scientific fact-checking

Health Economics & Real World Evidence

Burden of Illness (BOI) reports (clinical, humanistic, economic)
Systematic & Targeted literature reviews (SLR & TLR)
Epidemiology reports, literature searches and reviews
Real-World Evidence (RWE) reports
Patient-Reported Outcomes (PRO) assessments
Access evidence and value dossiers (AE&VD)
Health Technology Assessment (HTA) reports
Statistical analysis: Meta-analysis, Indirect treatment comparisons (ITC), Network meta-analysis (NMA)

Medical Affairs & Promotional Deliverables

Abstract booklets, brochures, newsletters, clinical compendiums
Advisory board meetings, steering committee meetings, satellite symposia
Competitor and treatment landscapes slide decks, competitive product analysis and summaries
Conference coverage and report writing, pre- and post-congress spotlight decks, publication alerts
Emailers, gap analysis, KOL management
Medical information deliverables, scientific response letters
Website creation and update
Whiteboard animations, HTML/articulate storyline, infographics, videos
Virtual instructor classroom trainings (VILTs)

Regulatory Affairs

Investigational New Drug (IND) submissions
New Drug Application (NDA) submissions
Clinical Trial Applications for Health Canada
FDA Meeting Packages
Clinical study protocols (CSP)
Informed consent forms (ICF)
Investigator brochures (IB)
Case report forms (CRF)
Clinical study reports (CSR)
Safety narratives & reports
Clinical summaries, Integrated safety summaries (ISS), Development safety update reports (DSUR)
Statistical analysis plans (SAP)
Patient recruitment materials

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