Please contact us: +49 (0)251 978240-0

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.

PRO-LIANCE GRÜNDER, 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.

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.

SCIENTIFIC & REGULATORY EXPERT
Dr. Sabine Bertsch holds a degree in biomedical science and, after completing her doctorate, worked in the field of medical device and drug evaluation and development. At PRO-LIANCE, she will draw on her experience to support clients in the development of safe and innovative medical devices.

REGULATORY & SCIENTIFIC EXPERT
As a biophysicist by training, Dr. Eva Danner enjoys working in an interdisciplinary setting. During her doctoral studies, she focused on biomedicine before shifting her focus to regulatory affairs. She will now apply her pragmatic and efficient approach at PRO-LIANCE to support clients with their clinical evaluations.

CLINICAL EVALUATION & PMS EXPERT
Dr. Leigh-Anne Dell-Brown is a neuroscientist with a PhD in neuroanatomy. She has extensive experience in scientific and medical writing as well as in presentations. She draws on her experience in the industry, her analytical skills, and her problem-solving expertise to provide clients with the best possible support.

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.

CLINICAL EVALUATION EXPERT
Dr. Thomas Gabriel is a biologist with a Ph.D. in neuroscience. He has been working in clinical research since 2011 and has assisted manufacturers in conducting clinical trials. Since 2018, he has also been preparing clinical assessments and will bring his experience to the PRO-LIANCE team.

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.

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.

CLINICAL EVALUATION EXPERT
Kanako Nishino holds a master's degree in pharmacy and has many years of experience as a consultant in the preclinical and clinical sectors of pharmaceutical and medical device companies. At PRO-LIANCE, she assists clients with clinical and biological evaluations.

REGULATORY AFFAIRS & QUALITY CONSULTANT
Dr. Johannes Prox holds a Ph.D. in biochemistry and is the author of various publications in the fields of neurology and immunology. Following his academic career, he gained experience in clinical affairs, regulatory affairs, and quality management at various companies in the medical technology and clinical research sectors. At PRO-LIANCE, he draws on his extensive experience to support clients in the development of innovative and successful medical devices.
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