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Event Type:
Workshops/Training Courses
Date:
Mar. 6-7, 2017
Location:
Basel
- Regulatory differences in the EU, US & regions of interest
- Sustainable product portfolio for generics & biosimilars
- Cost containment and procurement of generics & biosimilars
- Redesign & optimization of generics & biosimilar model
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Supergenerics vs generics
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Generic business development & risk reduction
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Creating new market segments
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Generics in 2020 and beyond
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Challenges of drug low prices and low margins
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Health policy implications and recent evolutions
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Approval pathways and registration issues
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Expanding role of the OTC market as an INN defense
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Interactive way of lecturing
through stimulation of discussions
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Individual case by case consultancy with the trainers
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Comprehensive printed and digital
course documentation
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8H+ of networking
with other industry experts
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Case studies from the trainer`s
experience
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Certificate of Completion
issued by the trainers
BY POSITION
- Product portfolio managers
- Business developers
- Strategic planners
- Heads of R&D
- Regulatory affairs
- Market access
- M&A
- Intellectual property
- Pricing & reimbursement
BY INDUSTRY
Pharmaceutical
- Generics
- Biosimilars
- Healthcare