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Produktbild: Principles of Biomedical Sciences and Industry
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Principles of Biomedical Sciences and Industry Translating Ideas into Treatments

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Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

17.08.2022

Abbildungen

Tabellen, schwarz-weiss, schwarz-weiss Illustrationen

Herausgeber

Markus Hinder + weitere

Verlag

Wiley-VCH

Seitenzahl

448

Maße (L/B/H)

25,1/17,7/2,7 cm

Gewicht

978 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-3-527-34571-7

Beschreibung

Portrait

Markus Hinder studied medicine at the Universities of Heidelberg, Paris and Zürich and obtained a doctoral degree in pharmacology from Heidelberg University. After graduation he trained in clinical pharmacology, cardiology and emergency medicine. He underwent postgraduate training in clinical trial methodology and statistics at the Universities of Basel and Brussels. He joined the pharmaceutical industry more than 20 years ago and held senior leadership positions in clinical pharmacology, translational medicine, clinical development, medical affairs and project management. He has been lecturing pharmacology and pharmaceutical R&D since 2004. In 2010 he was appointed professor at Cardiff University/ Hochschule Fresenius. He serves as a reviewer for several journals and associate editor for the Journal of Translational Medicine.

 

Alexander Schuhmacher graduated in biology from the University of Konstanz (Germany), in pharmaceutical medicine at the University of Witten/Herdecke (Germany) and did a Ph.D. in molecular biology at the University of Konstanz; he is also a graduate of the Executive MBA program at the University of St. Gallen (Switzerland). Alexander holds a full professorship in life science management at the Technische Hochschule Ingolstadt (Germany). His research focus is on biopharmaceutical innovation management with a specialization on R&D efficiency, artificial intelligence and open innovation. Prior to that, Alexander worked 9 years as professor at Reutlingen University (Germany) and 14 years in various R&D leadership positions in the pharmaceutical industry.

 

Jörg Goldhahn received his M.D. 1997 from the Friedrich-Schiller University in Jena, Germany, finished a postgraduate course (MAS) in Medical Physics and Biomechanics at the ETH Zurich in 2000, received the postdoctoral lecture qualification (Habilitation) in 2008 and became a faculty member of the department for health sciences and technology (D-HEST) as adjunct professor 2014. He worked as a translational medicine expert at the Novartis Institutes for Biomedical Research (NIBR) in Basel in addition to more than 15 years in clinical research. He is currently the head of the Institute for Translational Medicine and medical director of the bachelor in medicine at ETH in Zurich, Switzerland.

 

Dominik Hartl studied Medicine at the Universities of Regensburg, Munich and Melbourne and obtained his doctoral degree in Immunology from Munich/LMU University. He is board certified in Pediatrics and Infectious Diseases and worked as Physician Scientist/Post-Doc Scholar at Yale University. He joined the pharmaceutical industry more than 6 years ago and gained extensive experience in his positions in Drug Discovery, Translational Medicine, Biomarkers and Precision Medicine/Personalized Healthcare in Biotech and Big Pharma. In addition to working in the pharmaceutical industry, Dominik is a Professor for Pediatric Immunology/Infectious Diseases at the University of Tübingen.

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

17.08.2022

Abbildungen

Tabellen, schwarz-weiss, schwarz-weiss Illustrationen

Herausgeber

Verlag

Wiley-VCH

Seitenzahl

448

Maße (L/B/H)

25,1/17,7/2,7 cm

Gewicht

978 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-3-527-34571-7

Herstelleradresse

Wiley-VCH GmbH
Boschstraße 12
69469 Weinheim
DE

Email: wiley-vch@kolibri360.de

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Die Leseprobe wird geladen.
  • Produktbild: Principles of Biomedical Sciences and Industry
  • Biopharmaceutical Innovation at a Glance

    Pharmacology and Drug Targets - The Basis of Therapeutics

    Principles and Methods of the Pharmaceutical Drug Discovery Process - From Idea over Target to a Development Candidate

    Biomarkers - Definitions and Utility for Drug Development

    Toxicology and Managaing Safety and Risks

    Introduction to Chemistry Manufacturing and Controls - From Compound and Development Candidate to Drug

    Translational Medicine - The Bridging Discipline: Role and Tools in the Drug Development Process

    Decision-Making - What Are the Key Drivers Around Decision-Making in Drug Development?

    Clinical Drug Development - Clinical Characterization for Regulatory Approval

    Regulatory Affairs - Communicating with Health Authorities

    Regulatory Affairs in Device Development - How to Design Medical Devices Capable to Enter the Market

    Market Entry and Reimbursement - Making Drugs Available for Patients After Drug Approval

    Pricing in Germany - Key Learnings for Optimising Price Potential After the Introduction of AMNOG

    Project, Risk and Portfolio Management - Managing R&D Project Costs and Risks

    Intellectual Property - How to Protect Innovation in the Biopharmaceutical Industry

    Patents in the Biomedical Sciences and Industry - The Case of Swiss Life Science Company Prionics

    Pharmaceutical Business Development & Licensing - Overview of a Cross-functional and Multifaceted Role and Its Key Elements in Biopharmaceutical Industry

    The Entrepreneur's Guide Through the Galaxy of Biotech Funding

    Medical Technologies - Key Learning from Two Case Studies

    Diagnostics - Tools for Clinical Decision Making and Clinical Trial Endpoints

    Vaccination - Towards an Improved Influenza Vaccine