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Torsten Reinheimer

Torsten Reinheimer

Principal Scientist/Director Non-Clinical Develop.

Gesundheitswesen

Guntramsdorf, Mödling

Soziales


Über Torsten Reinheimer:

I have been employed in the pharmaceutical industry in Germany and Denmark for 22 years, with a focus on non-clinical research and development of peptides, and biologics, including pharmacology, 
safety pharmacology, pharmacokinetics, and toxicology. I have been engaged in several therapeutic areas including intensive care, cardiovascular and inflammatory diseases, reproductive science, gastroenterology together with liver diseases, immunology, and microbiome. I have contributed to and led international project teams successfully transitioning numerous drug candidates from preclinical or clinical phases to regulatory submissions in Europe and US.
Please consider me as Pharmacologist/Toxicologist ERT. I am an experienced drug developer with strong scientific background/network, familiar with non-clinical strategy design, safety assessments and influencing global multidisciplinary collaborations. Importantly, I have broad understanding monitoring multisite GLP studies, implementing disease models, translational PK/PD, CRO engagement, documentation filing/reviews (eCTD, IB), regulatory interaction (FDA, PEI), support 
management, manage stakeholders/external partners, build scientific evidence, and due diligences of external opportunities. 

Erfahrung

since 2020: Owner of reinheimer.expert ApS, Copenhagen, Denmark
Pharmacology, toxicology, pharmaceutical R&D consultancy
Advising a Danish biotech on toxicology strategy for an anti-CMV protein
Lecturer for pharmacology and toxicology at Döpfer University Germany
Advising a Swiss start-up on pharmacology and PK of a tocolytic drug
Advising an US start-up on their tox package for an antihypertensive
Advising a Chinese company on their tox strategy for an antiviral drug
Director/Principal Scientist Experimental Medicine/Non-Clinical Dev.


2002 - 2020 FERRING Pharmaceuticals A/S, Copenhagen, Denmark
a privately-owned, global, mid-sized pharmaceutical enterprise
2 billion € yearly turnover, ca. 7,000 employees worldwide
TAs reproductive medicine/maternal health, gastroenterology, urology
Responsibilities
• Design non-clinical strategies, safety pharmacology, PK/PD
• Principal pharmacologist/toxicologist, overall NC safety assessment
• Inspire, lead project teams/management; prepare development plans
• Leading role in health authority meetings
• Search new in-vitro, ex-vivo or animal models, manage CROs
• Build-up network of scientific advisors and academic centres
• Initiate/facilitate early-stage feasibility activities, experimental support
• Scientific support to Ferring research, endorse testing strategies
• Lead due diligences, provide scientific insight and final evaluations
• Innovation leadership, use patents and drug candidate profiling
• Coach pharmacologists and toxicologists, present lectures
Achievements
• Characterised terlipressin as a prodrug & its PK/PD characteristics
• Developed V1A antagonist in preeclampsia, improved foetal outcome
• Characterised quinagolide for non-hormonal endometriosis treatment
• Developed vasopressors to lower portal pressure in liver cirrhosis
• Characterised selepressin as anti-leakage, V1A-selective sepsis drug
• Microbiome replacement therapy to cure refractory C. diff. infection
• Developed olamkizept to treat chronic inflammatory bowel disease
• Characterised DNAase as treatment for male fertility or DNA damage
• Developed barusiban as OT-selective tocolytic in primates
• Life-cycle management of atosiban, a globally registered tocolytic
• Developed carbetocin for prevention of post-partal haemorrhage

Bildung

Since 2013 Registration as British/European toxicologist BRT/ERT
2008 - 2013 Master of applied toxicology with distinction, Postgraduate studies, University Surrey UK
2007 - 2023 Honorary professorship, Warwick Medical School, UK, Biomedical Research
since 1996 Qualification as pharmacologist approved by DGPT
since 1995 PhD-degree in neuropharmacology with magna cum laude 
1990 - 1997 Institute of Pharmacology, PhD student, Joh. Gutenberg-University Mainz
1984 - 1989 Qualification as pharmacist, Johannes Gutenberg-University Mainz
1970 - 1983 Matriculation standard, secondary school Groß-Gerau, Germany 

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