We understand the critical nature of Pharmaceutical Production and the need for reliable and efficient operations. Aryium works closely with key vendors, fostering strong relationships that enable us to deliver proven technology and mission-critical solutions for your production facility.

Our key skills encompass primary and secondary Pharmaceutical Production, including API production and fill-finish processes. We are well-versed in quality control methodologies, covering in-line, end-of-line, on-site, and off-site quality control procedures. Our team is experienced in designing aseptic environments that adhere to Annex 1 standards, ensuring the highest level of sterility.

Aryium specialises in integrating ISO cleanroom classifications, ranging from ISO 9 to ISO 1, into your Pharmaceutical Production facility. We are skilled in working with cleanroom grades CNC to A, ensuring the controlled environments necessary for pharmaceutical production.

We have expertise in integrating Electronic Batch Records (EBR) and Process Analytical Technology (PAT) to enhance efficiency and data management within your production processes. Our team is well-versed in biocontainment practices, ranging from Containment Level 2 (CL2) to Containment Level 4 (CL4), enabling us to design facilities that handle genetically modified materials and in ATEX to ensure safety in explosive environments.

We understand the specialised requirements of CAR-T and monoclonal antibody (mABs) production and can provide tailored solutions for these processes. Whether you require retrofitting of existing facilities or the design of greenfield or brownfield sites, Aryium has the expertise to meet your specific needs.

At Aryium, we are committed to delivering Pharmaceutical Production facilities that adhere to regulatory standards, optimise operations, and support your growth in the global market. Our collaborative approach and attention to detail ensure your facility is designed for success.