Articles
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Overcome Common Pre-Filled Syringe Challenges Through Partnership
5/23/2025
The pre-filled syringe space is one of the fastest growing pharma sectors, offering greater patient safety and lower manufacturing costs. But pre-filled doesn’t translate to easily filled; there are particular obstacles to overcome.
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Drug Product Manufacturing: Scaling Product From Bench To Market
5/7/2025
Curia offers comprehensive development and manufacturing services to meet needs through the entire lifecycle of your sterile drug product. Leverage our in-depth expertise and capabilities at any scale, from early clinical through large-scale commercial.
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Sterile Fill/Finish Services
3/25/2025
Our 87,000 sq. ft. cGMP-certified drug product manufacturing facility, located in Baltimore, Maryland, offers aseptic fill/finish manufacturing of biologics and sterile injectables.
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Bringing Commercial Success To Our Partners Through Our Broad OSD Expertise
3/25/2025
By combining deep scientific expertise with cutting-edge technology, we ensure the safety and effectiveness of each formulation through precise control of API release.
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Supporting Global Pharma Partners With Flexible, Reliable Solutions
3/25/2025
As a leading CDMO, we specialize in the development and manufacturing of diverse dosage forms for both clinical and commercial applications, driven by a culture of innovation and commitment to quality.
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3D Screen Printing: Enabling A New Generation Of Complex Formulations
3/17/2025
Screen-Printed Innovative Drug Technology can produce oral, transdermal, and implantable dosage forms while ensuring heterogeneous distribution of active ingredients.
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Vial Fogging: Practical Considerations For Vial Selection
10/16/2024
Vial fogging is a common phenomenon observed in lyophilized biologic drug products. This document presents two case studies that explore critical factors contributing to vial fogging and inform vial selection decisions.
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Stopper Migration In Frozen Pre-Filled Syringes
10/16/2024
Review a semi-automated method for dynamically assessing plunger migration under controlled variations in temperature and pressure, utilizing computer vision tools.
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Methods For Determining Equipment Capability Of Freeze-Dryers
10/16/2024
Observe two experimental methods for determining choked flow: the minimum controllable pressure method and the choke point method.
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Leak Rate Testing for Freeze Dryers: A Scientific Approach
10/16/2024
Explore our innovative approach to establishing leak rate acceptance criteria and ensure the integrity of your freeze-drying processes for sterile pharmaceutical production.