Tim Kortum

Tim Kortum is a seasoned pharmacovigilance professional with over a decade of comprehensive experience in the pharmaceutical industry. Currently serving as a Freelance Consultant in Pharmacovigilance and Drug Safety at Evolve Pharma Consultancy, Tim leverages his extensive expertise to support pharmaceutical companies in ensuring compliance with global safety regulations and optimizing their drug safety processes. His role involves providing tailored pharmacovigilance services, including ICSR management, aggregate report writing, signal detection, and risk management strategies, either remotely or on-site. Tim’s flexible approach allows him to adapt to the unique needs of each client, offering part-time on-site support outside the Netherlands when necessary.

At Evolve Pharma Consultancy, Tim has been instrumental in leading key projects that enhance pharmacovigilance systems and streamline safety reporting workflows. His deep understanding of clinical development, combined with his proficiency in data analysis and regulatory submissions, enables him to deliver actionable insights that mitigate risks and support regulatory compliance. Tim’s expertise spans across various therapeutic areas, notably oncology and life sciences, where he applies his knowledge of molecular biology and clinical trials to improve drug safety monitoring.

With a strong foundation in industry standards such as ICH-GCP and a keen eye for detail, Tim ensures that all safety data is accurately captured and analyzed to support robust pharmacovigilance activities. His skills in data analysis, combined with his proficiency in tools like Microsoft PowerPoint and WordPress, allow him to communicate complex safety information effectively to diverse stakeholders. Dedicated to maintaining the highest standards of drug safety, Tim Kortum continues to be a valuable asset to clients seeking expert guidance in pharmacovigilance and drug safety management.