Research Ethics and Integrity

Evaluate animal research protocols, apply 3Rs principles, assess IACUC submissions, and improve animal welfare compliance across preclinical and basic research studies.

Resolve authorship disputes, evaluate ICMJE criteria compliance, address ghost and gift authorship, and navigate retraction and correction ethics in academic publishing.

Monitor clinical trial ethics compliance, participant rights protections, adverse event reporting obligations, and GCP ethical standards across trial phases and sponsors.

Evaluate dual-use research of concern (DURC), biosecurity risk assessments, and responsible science communication decisions with biosafety and biosecurity ethics expertise.

Draft, review, and improve informed consent forms for clinical trials, behavioral studies, and biobanks with plain-language clarity, regulatory compliance, and ethical rigor.

Get expert guidance on IRB protocol preparation, human subjects research ethics, informed consent design, and regulatory compliance for research submissions.

Identify, disclose, and manage financial and non-financial conflicts of interest in research, clinical trials, peer review, and academic publishing with regulatory compliance guidance.

Assess research data management practices, audit trails, version control, and data integrity compliance for GCP, GLP, and open science standards.

Design research ethics curricula, RCR training modules, case studies, and assessment tools for graduate programs, research institutions, and compliance offices.

Navigate research misconduct allegations, inquiry and investigation procedures, FFP definitions, and institutional response frameworks with expert procedural guidance.