Passion for your process, product and patients

Therapure Biomanufacturing is a contract development and manufacturing organization (CDMO) that places product quality and patient safety at the forefront.

A key aspect related to product quality, and one of the final steps in the manufacturing process, is aseptic fill/finish. Therapure’s state-of-the-art cGMP facility supports aseptic fill/finish of your biologic and small molecule products from clinical trial material through to commercial manufacturing.

We provide the following services for aseptic fill/finish of your high-value drug product:

Vial Filling

  • Peristaltic pump–based systems, which use a disposable fill configuration with minimal line loss
  • High degree of accuracy and ability to fill small volumes
  • Wide range of batch and vial sizes



Integrated lyophilization capabilities for clinical and commercial products

  • Tofflon
    • 81 ft2 (7.5 m2)
    • 7 shelves
    • Temperature range -70°C to +80°C
  • IMA
    • 43 ft2 (4.0 m2)
    • 5 shelves
    • Temperature range -70°C to +80°C”

As part of our integrated quality systems, our team performs 100% visual inspection of the drug product containers prior to labeling, which is followed by packaging and cartoning. As well, we have the ability to develop and execute ICH-compliant stability protocols.

Your high-value finished product is stored in our cGMP warehouse and shipped using validated shipping protocols for next-day North American delivery to your clinical or commercial sites.