Landing EU Pharma

Landing EU Pharma
Product Description

Marketing authorization is granted only to an EU-based applicant. Medicines imported into the EU must be QC tested and QP batch-released before entering the EU. Our QP and EU batch release services can assist you with EU imports of sterile and non-sterile medicinal products, as well as ATMP and IMP.

The QbD Group can assist you with a single QC or regulatory question, but we can also take over the entire process of registration of your medicines in the EU, QC analysis, import, and batch release as outlined below. 

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Quality by Design NV

  • Country/Region:
    Belgium
  • On CPHI since:
    2022
  • Certificates:
    4
  • Employees:
    500 - 999
Company types
Consultancy
Primary activities
Laboratory Services
Medical Devices
Pharmaceutical Company (generic finished products)
Regulatory Affairs
Technology
View company profile
Categories
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Specifications
  • Details
    Are you looking for EU-GMP Import services to support your business? The QbD Group is GMP licensed and can support all steps of importing your products, including QC and QP services.
  • Supplied from
    Belgium
More specifications Fewer specifications
Sales Markets
Show more Show less

Quality by Design NV

  • Country/Region:
    Belgium
  • On CPHI since:
    2022
  • Certificates:
    4
  • Employees:
    500 - 999
Company types
Consultancy
Primary activities
Laboratory Services
Medical Devices
Pharmaceutical Company (generic finished products)
Regulatory Affairs
Technology
View company profile

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Quality by Design NV resources (1)

  • Landing EU Pharma

    Brochure Landing EU Pharma

    The regulatory landscape to successfully launch your products in the EU​. QbD Group is your life sciences partner for EU market access. ​Discover our Global-Pharma solutions, including our Vigilance Services, European market entry guidance, our Lab Services, and Toxicology Services.​