MEDIUS AG - DRUG REGULATORY AFFAIRS SERVICES SWITZERLAND
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Medius AG

Meet your team of skilled experts for a highly professional experience.

Dr. Urs Rickenbacher
Ph.D. in toxicology at the Swiss Federal Institute of Technology (ETH) in Zurich,
research in medicinal chemistry at the National Institute of Environmental Health Sciences (NIEHS), USA, more than 30 years of experience as DRA manager, founder and managing director of Medius AG.
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Franziska Hüsler, Dipl.-Ing. FH (external)
Biotechnology engineer with 10 years of experience in quality assurance (QA) and as RP in the pharmaceutical industry, with more than 3 years of experience in QA in medical devices industry (ISO 13485) and more than 5 years of experience as head of the regional medicines inspectorate of North-Western Switzerland and GMP/GDP-inspector including narcotics. Founder and managing director of Hüsler Consulting GmbH. With Medius since 2022.
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Dr. Géraldine Bouchard-Doulakas
Ph.D. in chemistry at the University of Lausanne, master in physical-chemistry at the Federal Institute of Technology in Grenoble, 3 years senior teaching assistant, more than 16 years of industry experience in CMC and Regulatory Affairs Management, with Medius since 2012.
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Arina Mathys, M.Sc.
Master in Chemistry at the University of Applied Sciences of North-Western Switzerland and Molecular Biology at the University of Basel, 7 years of laboratory and research experience, more than 12 years of regulatory affairs and quality management experience, with Medius since 2012.  Contact
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Dr. Jolanda Ceresa
Ph.D. in analytical chemistry at the Swiss Federal Institute of Technology (ETH) in Zurich; employment as project leader and quality assurance manager, more than 10 years of experience in quality affairs (GMP/GDP) in pharmaceutical and cosmetics industry, with Medius since 2019.
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Manuela Bartsch, M.Eng.
Bachelor & Master of Engineering in Pharmaceutical Technology and Quality Management at the Universities of Applied Sciences (FH) Anhalt & Wismar in Germany, more than 10 years of industry experience in pharmaceutical manufacturing and process engineering; 10 years experience as quality manager and RP, with Medius since 2019.
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Barbara Pauli, MSc, MAS IP
Master of Biology II (University of Basel) and Master of IP (Swiss Federal Institute of Technology in Zürich). More than 15 years of experience in global regulatory requirements and procedures from drug development through approval and product lifecycle management, with Medius since 2022.
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Cinzia Müller
10 years of experience as assistant sales manager, more than 20 years of experience as regulatory affairs assistant and case manager, with Medius since 2000.
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Dorothea Glauser
More than 35 years of experience as regulatory affairs assistant and case manager, with Medius since 2010.
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Medius AG
Drug regulatory affairs and development
Neue Bahnhofstrasse 160
4132 Muttenz
Switzerland

+41 61 465 70 40 - Phone
+41 61 465 70 41 - Fax
welcome@medius.ch

Office Hours
Mo - Fr
08.00 am - 05.30 pm
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Relevant Swiss law and ordinances
Federal Act on Medicinal Products and Medical Devices
​Ordinance on Licensing in the Medicinal Products Sector
​

Swiss competent authorities
​Swissmedic
Federal Office of Public Health

USA
FDA - USA Food and Drug Administration

EU
European Medicines Agency

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  • Home
  • Team
  • Services
    • Areas of Expertise
    • Market Entry
  • Experience
  • Customers
    • Client Profile
    • Client Satisfaction
    • Downloadarea
  • Career
  • Newsblog
  • Contact
    • Imprint
    • Privacy
    • Privacy note PV, MI and PC