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Prespack Sp. z.o.o.

About Prespack Sp. z.o.o.

Prespack specializes in contract packaging services, as well as the serialization and aggregation of medicinal products, products containing controlled substances (psychotropics), and products requiring cold chain storage. We are a family business founded by three brothers: Jacek, Stanisław, and Filip. Their values, consistent communication, and partnership-oriented philosophy add significant value for our clients.
Outsourcing secondary contract packaging services (CPO) at Prespack involves comprehensive support for pharmaceutical entities. 

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Certifications
  • GMP
    GMP
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Sales Markets
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Categories
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  • Country/Region:
    Poland
  • On CPHI since:
    2021
  • Certificates:
    1
  • Employees:
    50 - 99
Company types
Contract Service
Primary activities
Contract Manufacturer
Contact info
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Meet us at

CPHI Milan 2026

Fiera Milano, Italy
6 Oct 2026 - 8 Oct 2026
View Exhibitor Profile

Products from Prespack Sp. z.o.o. (4)

  • 2°-8°C storage

    Product 2°-8°C storage

    Storage of cold chain products (+2°C to +8°C) in a refrigerated chamber equipped with a dual cooling system and backup power, for further packaging or repackaging.

  • AGGREGATION

    Product AGGREGATION

    Pharmaceutical aggregation for markets in the Commonwealth of Independent States (CIS), Brazil, the USA, and Turkey. This service ensures product traceability at the collective packaging level, linking serialized individual product packages with higher levels of collective packaging, such as cartons an...
  • CONTRACT SECONDARY PACKAGING

    Product CONTRACT SECONDARY PACKAGING

    Outsourcing secondary contract packaging services (CPO) at Prespack involves comprehensive support for pharmaceutical entities. We operate under a Manufacturing/Importation Authorization for medicinal products and a Certificate of GMP Compliance (Good Manufacturing Practice) issued by the Chief Pharmac...
  • SERIALISATION

    Product SERIALISATION

    9 February 2019 saw the entry into force in Poland of Commission Delegated Regulation (EU) 2016/161 which requires medicinal product manufacturers to use certain safety features on their products. This posed a serious challenge to pharmaceutical and contract manufacturers who had to bring their manufa...