OUR TEAM
Meet the team
We are PRO-LIANCE
Florian Tolkmitt
PRO-LIANCE FOUNDER, REGULATORY & CLINICAL EVAL. EXPERT
Florian Tolkmitt is one of the founders and managing directors of PRO-LIANCE. Within the team he is responsible for Clinical Evaluation, Technical File and Risk Management. As a creative mind, he is always setting new impulses in the company and therefore ensures the continuous development of all employees. With the needs of the customer in focus, he is always looking for new solutions.
Dr. Thomas Brzoska
PRO-LIANCE FOUNDER, SCIENTIFIC & CLINICAL AFFAIRS EXPERT
Dr. Thomas Brzoska, a Doctor of Chemistry, is one of the founders of PRO-LIANCE and contributes profound knowledge from more than 250 CERs/BERs to the areas of regulatory affairs, risk management and quality management, among others. Looking back on many years of expertise, he is a huge support to the entire team when it comes to very tricky tasks. He considers it a challenge to transform complicated regulatory requirements into workable solutions for the customer.
Dr. Martin Bauer, MD, FNWC
MEDICAL EXPERT
After several positions in the pharmaceutical and biotech industry as Head of Clinical Development and Sr. Medical Director, Dr. Martin Bauer, who is also anesthesiologist and emergency physician, supports PRO-LIANCE as Medical Expert in the areas of Strategy, Safety and Medical Affairs. His knowledge in life cycle management and international drug development as well as his experience with the respective authorities (FDA, EMA, BfArM, MHRA, CDSCO) is of great value to our clients.
Dr. Sabine Bertsch
CLINICAL & REGULATORY EXPERT
Dr. Sabine Bertsch studied biomedicine and worked in the field of evaluation and development of medical devices and pharmaceuticals after her PhD. At PRO-LIANCE she will use her experience to support clients in the development of safe and innovative medical devices.
Dr. Eva Danner
SCIENTIFIC & REGULATORY EXPERT
As a graduate biophysicist, Dr. Eva Danner enjoys working interdisciplinary. In her doctorate, she focused on biomedicine and then started on regulatory affairs. She will now use her pragmatic and efficient approach at PRO-LIANCE to support customers in their clinical evaluation.
Dr. Anke Dopychai
CLINICAL EVALUATION EXPERT
Dr. Anke Dopychai is a biologist and holds a doctorate in pharmacology. Through further training, she gained additional qualifications as a TÜV-certified quality and project manager. She joined the PRO-LIANCE team in mid-2021 as an author for clinical evaluations and supports clients in the area of risk management.
Dr. Thomas Gabriel
CLINICAL EVALUATION EXPERT
Dr. Thomas Gabriel is a biologist with a doctorate in neuroscience. He has been working in clinical research since 2011 and has supported manufacturers in conducting clinical trials. Since 2018, he has also been creating clinical evaluation reports and will bring his experience to the PRO-LIANCE team.
Dr. Sabine Klugbauer
SCIENTIFIC & REGULATORY EXPERT
Dr. Sabine Klugbauer, a molecular biologist with a PhD, has many years of experience in the regulatory affairs of medical devices of various classes, gained at manufacturers and consulting service providers. She applies her expertise primarily to clinical evaluations, post-market surveillance (PMS with PMCF and vigilance), biological evaluations and technical documentation.
Dr. Raquel Marcos Esteban
SCIENTIFIC & REGULATORY EXPERT
Dr. Raquel Marcos Esteban is a Doctor of Chemistry and holds an additional MSc in Marketing and Customer Relationship Management. At PRO-LIANCE, she supports manufacturers in the areas of Clinical Evaluation and Clinical Follow-up (PMS/PMCF), as well as Post-Marketing Surveillance, preparation of SSCPs and also advises customers with regard to SOPs.
Dr. Sabine Mayer-Lambertz
CLINICAL & SCIENTIFIC EXPERT
Dr. Sabine Mayer-Lambertz studied biology and has a PhD in infection immunology. Following her academic career, she gained experience as a consultant in the field of clinical and regulatory affairs. Since the beginning of 2025, she is part of the PRO-LIANCE team, using her expertise to support clients as a clinical and scientific expert in the approval of medical devices.
Dr. Franziska Meyer
CLINICAL EVALUATION EXPERT
Dr. Franziska Meyer holds a PhD in biology/biochemistry with focus on biomedicine. At PRO-LIANCE she combines her experiences as a Medical Writer and QM consultant as a Clinical Evaluation Expert.
Dr. Fernando Muñoz Lobato
CLINICAL & SCIENTIFIC EXPERT
Dr. Fernando Muñoz Lobato holds a BSc in biochemistry and a PhD in biomedical research. With over 12 years of research experience in the fields of neuroscience and oncology, and 4 years of experience helping companies bring their innovations to the market, he joined PRO-LIANCE at the beginning of 2022 to support our clients with Clinical Evaluations, Biological Evaluations and Project Management.
Dr. Katharina Sophie Neuhäuser
SCIENTIFIC, REGULATORY & QUALITY EXPERT
Dr. Katharina Neuhäuser holds a degree in biotechnology/biochemistry and a PhD in biomedicine (radiation oncology). At PRO-LIANCE, she is responsible for Clinical Evaluation, Post-Market Surveillance and Technical Documentation. Currently, she is also establishing and coordinating an R&D project. She picks up new knowledge quickly and is very creative. AS a result, she always finds efficient solutions to support customers in the best possible way.
Kanako Nishino
CLINICAL EVALUATION EXPERT
Kanako Nishino holds a Master’s degree in Pharmacy and has many years’ experience as a consultant in pre-clinical and clinical field of pharmaceutical and medical device companies. At PRO-LIANCE she supports clients with a Clinical and Biological Evaluation.
Dr. Johannes Prox
REGULATORY AFFAIRS & QUALITY CONSULTANT
Dr. Johannes Prox holds a PhD in biochemistry and is author of various publications in the fields of neurology and immunology. After his scientific career he gathered experience in the fields of regulatory affairs, clinical affairs and quality management working for medical technology and clinical research companies. At PRO-LIANCE he will use his experience to support costumers in developing innovative and successful medical products.
Dr. Christine Stock
CLINICAL EVALUATION EXPERT
Dr. Christine Stock studied biotechnology and received her PhD in the field of immunology in preclinical research for a pharmaceutical company. After further training in the field of clinical studies, she has been working as a medical writer for medical devices for several years and has extensive expertise and several years of experience in the preparation of clinical evaluations for medical devices.