Sterile Drug Product

Albany, NY- October 27, 2025 – Curia, a leading global research, development and manufacturing organization, today announced the completion of a $4 million investment to upgrade its two API aseptic suites in Valladolid, Spain. The investment aligns with the latest EU GMP Annex 1 standards and reinforces Curia’s longstanding commitment to regulatory excellence and product quality. Annex 1 provides general guidance for the design and control of facilities, equipment, systems, and procedures used for the manufacture of all sterile products, applying the principles of Quality Risk Management (QRM) to prevent microbial, particulate, and endotoxin contamination in the final product.

Flow Chemistry

The Glasgow, UK, site is well known throughout the industry for its more than 25 years of experience with formulation, lyophilization development and sterile fill-finish capabilities, including ADCs and other highly potent products. The current expansion is expected to be completed by early 2027. The investment will add an Annex 1 compliant isolator-based vial filling line and lyophilizer. Once complete, Glasgow will be able to fill batches up to 20,000 vials and will be well‑positioned to support future small‑scale commercial fills.

Curia designs and scales microbial fermentation and biocatalytic processes, coupled with advanced chemical synthesis to deliver safer, greener and more cost‑eff

Curia overview of product and services.

Curia (formerly AMRI) has development and clinical drug substance teams who exceed expectations on even the most challenging projects. Working in state-of-the-a

Curia Fine Chemical Catalog

Curia Biologic Service

API Catalog

Sterile Drug Product Fact Sheet

Curia corporate overview.

Curia API Catalog

Curia Biologics Discovery fact sheet

Curia Small Molecule Fact Sheet

Curia Sterile Drug Product Fact Sheet