CLT – consulting services

Medical monitoring pharmaconvigilance Safety Committees

Supporting smarter safety decisions

Independent medical consulting for Pharma, Biotech, and CROs across Scandinavia and Europe.

CLT Vigilance Consulting supports sponsors and CROs in safeguarding patient safety and ensuring the medical integrity of clinical trials/clinical investigations and marketed products.

Combining clinical experience, regulatory know-how, and operational insight, Cornelia Lif-Tiberg, MD, provides independent expertise in Medical Monitoring, Pharmacovigilance, strategic Medical Advisory, and independent Safety Committees.

The focus is simple: protect patients, defend data quality, and enable confident and ethical decisions.

Proactive oversight, not reactive reporting

Clinical safety is most effective when risks are identified early, escalated clearly, and documented to high regulatory and quality standards.

Experience across the full safety chain

Cornelia combines hands-on clinical decision-making from anesthesia and intensive care with years of operational responsibility in contract research and drug development. This allows her to interpret safety events in context — medically, operationally, and regulatorily.

Medical Monitoring

Centralized medical oversight in clinical trials: AE/SAE review, eligibility guidance, protocol compliance, safety signal assessment.

Pharmacovigilance

Clinical evaluation of individual cases and cumulative data, including signal assessment and regulatory safety reporting.

Medical Advisory

Senior medical input for study design, protocol development, escalation decisions, and sponsor-facing communication.

Safety Committees

Independent safety review, Safety Committee/DMC participation, and structured benefit–risk recommendations.