We specialise in designing and constructing facilities that provide controlled environments for conducting rigorous trials and research studies. Our team is well-versed in creating small-scale product development facilities and pilot plants that facilitate pharmaceutical product development, validation, and quality checking.

Our facilities encompass quality control/quality assurance laboratories and development laboratories that meet the highest industry standards.

Our team is skilled in creating aseptic suites and radioactive suites that adhere to stringent standards for the handling of pharmaceutical substances. Additionally, we have experience in developing tropical diseases and quarantine suites that support research in specific regions and diseases.

Aryium places great emphasis on adhering to Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards to support the integrity and reliability of Pharmaceutical Research. Our expertise in ISO cleanroom classifications, from ISO 9 to ISO 1, enables us to create controlled environments that meet the specific requirements of Pharmaceutical Research processes. We are experienced in working with cleanroom grades CNC to A, ensuring that our facilities meet the highest cleanliness and contamination control standards, and have the relevant biocontainment expertise to support live vaccine development.

At Aryium, we are dedicated to delivering Pharmaceutical Research facilities that foster innovation, adhere to stringent regulations, and contribute to advancements in the field. Our collaborative approach and attention to detail ensures that your facility provides a safe and conducive environment for critical Pharmaceutical Research.