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Regulatory Affairs
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Pricing and reimbursement of drugs
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Process analyses and improvement of pharmaceutical
logistic chains
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Total
Quality management and GCP, GLP and GMP,
Pharmaceutical Qualityassurance, Audits
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Quality Assurance: SOPs and documentation
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Medical Affairs incl. Clinical Trial Management,
Clinical Development and Monitoring
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Pharmacovigilance
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Medical Information Services
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New-product development: PARACELSUS data base
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Project management for herbal and orphan drugs
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Business Development
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Expert opinions for the Austrian Federal Ministry for
Public Health-BMGFJ, AGES PharmMed as non authority
expert
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Qualification as Managing director according to Austrian
trade regulations for manufacturing of drugs, drug
distribution and trade with good of all kinds (medical
devices and diagnostics) as well as Technical office and
as management consultant in the field of the
pharmaceutical industry.
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Training courses, Workshops and Presentations.