Freeze drying

Freeze drying
Product Description

The value proposition generated through two sites specialized in freeze drying is unique, from manufacturing process optimization to producing freeze dried characterized and documented vials, allowing our clients to diff erentiate on their own markets. We recently invested 7 million euros to increase capacity in our Spanish site targeting specialization in freeze dried and F&F sterile products compliant with new GMP Annex 1. We can offer a capacity of 30 million vials. Meribel Pharma Solutions has a dedicated center of excellence with 15 freeze driers and laboratory equipment to simulate cycles, with QBD expertise mastering the entire cold chain. We developed the capability to install new capacities in less than 12 months. Recently, we got FDA approval for one of our major API product. Following an audit of the manufacturing process by the US authorities, we obtained prior approval to manufacture commercial lots for US patients. One crucial fact is that we obtained this a...

Meribel Pharma Solutions

  • Country/Region:
    France
  • Founded:
    2024
  • On CPHI since:
    2015
  • Certificates:
    4
  • Employees:
    1000 - 4999
Company types
CMO/CDMO
Primary activities
Contract Manufacturer

Meribel Pharma Solutions

  • Country/Region:
    France
  • Founded:
    2024
  • On CPHI since:
    2015
  • Certificates:
    4
  • Employees:
    1000 - 4999
Company types
CMO/CDMO
Primary activities
Contract Manufacturer

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  • OTC and MD dossiers

    Product OTC and MD dossiers

    A list of regulatory OTC dossiers compliant with European regulations and in CTD structure (NEES-eCTD) is available. These dossiers are ready to be audited by clients and to be submitted for registration to Health Authorities. We provide support during the registration process until the dossiers are author...

Meribel Pharma Solutions resources (1)

  • Brochure Meribel Pharma Solutions Corporate Brochure Capabilities

    Navigating complexities togetherWe’re a niche player, mid-size CDMO dedicated to providing exceptional quality and efficient timelines.

    With specific capabilities and an integrated network across Europe, we offer the extensive expertise in development needed to ensure a seamless journey from concept to commercialisation, and a particular specialisation and deep knowledge in sterile multidoses, sterile and non-sterile lyophilised products and API, sachets and stick packs.

    We deliver comprehensive support for the production of oral solid dose, liquid and semi-solids.

    No matter the challenge, we are here to help you through every step of your journey.