Small Molecules >> Pharmaceutical Manufacturing >> Non-Aseptic Fill and Finish

Non-Aseptic Fill and Finish

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Eurofins BioPharma Product Testing Netherlands provides non-Aseptic Manufacturing services for pharmaceutical products. Our process is a customized one, resulting in flexibility that allows solutions in a wide range of compounds, primary packaging systems, batch sizes and fill volumes.

Customized Manufacturing of small scale batches

Our expertise lies at manual small scale GMP manufacturing of liquid or powder, sterile or non-sterile products. The non-sterile manufacturing can be done in our Feasibility lab or in our cleanroom, Class C environment. Services include

  • Capsule filling – filling of powder or granulles in soft gel capsules
  • Liquid or powder fill, in bottles, infusion bags, multi-doses flasks
  • Clinical trial material (all phases)
  • Small scale commercial batches

Services are delivered in a wide range of volumes and packaging systems and to a large array of product types. Our manual techniques gives you great flexibility in your requirements.

Available primary packaging and fill volumes

Eurofins BioPharma Product Testing Netherlands performs non-Aseptic Manufacturing activities, either with a ready-to-fill bulk, or with compounding based on your recipe. If necessary, the compounding process can be designed in close collaboration with us.

As all steps in the process are executed (semi-)manually, services can be offered for the following packaging systems and volumes.


Do you require other packaging systems or volumes? Discuss your needs to find a solution together.

Why choose Eurofins BioPharma Product Testing

  • Full GMP manufacturing services in-house available. Eurofins BioPharma Product Testing Netherlands can guide clients through their entire pharmaceutical development process.
  • Manual Fill & Finish. A manual approach allows for great flexibility in the process. Contact us if you have specific requirements.
  • Release Testing & Stability Study. Testing of Drug Products is our core business. We can help you in the Qualification and Validation of your methods, perform release testing of your product, and deliver the stability data needed for filing.
  • Wide range of related services. We can select, purchase and release (EP and USP) your raw materials and excipients. We can release your product for use in the clinic (Batch Certification) and we can help you with labelling, packaging and distribution (GDPR) of your product.