As a Medical Monitor at Confidence Pharmaceutical Research, Dr. Katarina Nedman oversees every stage of our clinical trials, from protocol development to data analysis. Her meticulous attention to detail and unwavering commitment to Good Clinical Practice (GCP) guidelines ensure that our trials are conducted with the utmost safety and scientific rigor.
Dr. Nedman’s expertise is invaluable in identifying potential safety concerns, reviewing adverse events, and making informed decisions about study design and modifications. She acts as a vital bridge between the scientific community, regulatory authorities, and the people we serve.
Her extensive educational background is primarily focused on medical science and pharmacovigilance. Katarina furthered her education by pursuing a Doctor of Philosophy (PhD) in Medical Science at Lund University, specializing in Medical Writing for Clinical Trials and Regulatory Submissions.
In addition to her formal degrees, Katarina has completed countless certifications and courses related to pharmacovigilance, drug safety, research ethics, and clinical research from institutions like the European Program in Pharmacovigilance and Pharmacoepidemiology, the Faculty of Pharmaceutical Medicine of the Royal College of Physicians (UK), and the NIDA Clinical Trials Network.
Dr. Nedman’s commitment to advancing medicine extends beyond the walls of the lab. She is a passionate advocate for patient education and in her personal time she offers personal educational support for women after cesarean sections. She is also multilingual, fluent in English, Spanish, Swedish, and her native Russian.
At Confidence Pharmaceutical Research, we’re proud to have Dr. Nedman as a member of our team. Her expertise, passion, and unwavering commitment to patient safety are integral to our success.
