
Arman Ergenekon brings over 15 years of cleanroom industry experience within aseptic and GMP compliant manufacture of TGA-licenced products to TRI. An expert in GMP processes and manufacturing, Arman provides knowledge and guidance to Cleanroom tenants in areas such as training, quality control and assurance. Tenants also benefit from his strong regulatory experience gained from having established and managed a QMS and being involved in various TGA audits for multiple sites and products.
Arman and his entire team are committed to the progress of cutting edge research and development through the translational pathway, from bench to bedside, increasing access to the best possible medical research outcomes and improved quality of life for people suffering from illness.
Through collaboration and support for tenants, especially for organisations who are new to the GMP manufacturing industry, the TRI cleanrooms are geared to servicing the translation of innovation, while strengthening and interfacing research links to industry and government.
The TRI Cleanrooms are currently supported by a dedicated team with a broad range of knowledge and expertise across manufacturing of various products.
The expert staff are familiar with an extensive list of regulatory compliance requirements, and available to help facilitate and onboard cleanroom operations into our facility, and support the translation of discovery science through the cleanrooms and beyond.