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  • Product Development
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    • BE study
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    • Dossier lifecycle management
    • eCTD, NeeS publishing
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    • Rx to OTC switch
    • Scientific advice
    • Super-grouped Variations
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    • Variation Type I
    • Variation Type II
    • Grouped Variations
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    • QA Policy Development
    • Qualified Person for BR
    • Validation Protocol Development
  • Vigilance & Safety
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    • International pharmacovigilance
    • National pharmacovigilance
    • Literature Monitoring
    • Periodic Safety Update Reports
    • Risk Managment Plan
    • Validated PV database
  • Market Access
    • International market access support
    • National market access support
    • P&R support for generics
    • P&R support for innovative medicines
    • Pharmaco-economic study
  • Sales
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    • Communications to Payers
    • Licensing
    • Social Media Communications
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