Regulatory Affairs

Regulatory Affairs
Product Description

Nuvisan GmbH provides wide range of pharmaceutical services which includes regulatory affairs. Benefits: extensive experience with pharmaceutical start-ups, from contract research organisations to large pharmaceutical companies experienced with a wide range of product types including chemical drug substances, herbal preparations and biotechnology products. Strategy and planning: regulatory strategy consultation and guidance; development planning; expert review of scientific documents including gap analysis; interpretation of regulations and guidelines. Contact us for more information.

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Nuvisan GmbH

  • DE
  • 2015
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Contract Service
View company profile

Nuvisan GmbH

  • DE
  • 2015
    On CPHI since
  • 2
    Certificates
  • 1000 - 4999
    Employees
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Contract Service
View company profile

More Products from Nuvisan GmbH (18)

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    Product Oncology Centre of Excellence

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    Product Pharmacovigilance

    Nuvisan GmbH provides wide range of pharmaceutical services which includes pharmacovigilance. Contact us for more information.
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    Product Phase I Unit

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    Product Training

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  • Early Phase Clinical Study Expertise

    Product Early Phase Clinical Study Expertise

    State-of-the-art phase I/ll unit supporting complex clinical trials • First in Human ( FIH) to Proof of Concept ( PoC) • Clinical pharmacology studies through all phases • In-house safety lab and bioanalytical services • Special patient populations (with a focus on respiratory) • Data m...
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    Product Manufacturing, packaging & distribution service

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    Product Analytical Development & QC

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show all 18 other products

Nuvisan GmbH resources (1)

  • Chemical Development Solution

    Brochure Chemical Development Solution

    NUVISAN`s scientific team has extensive knowledge in the development of chemical processes up to GMP manufacturing for pre-clinical and clinical studies. We specialize in developing and manufacturing active pharmaceutical ingredients (APIs) and intermediates, offering support from early-stage R&D to commercialization.