• Clinical Research Organisation

Accelagen is a Melbourne based Contract Research Organisation (CRO) working with an array of local and international clients. Our services and expertise are helping facilitate the development of novel pharmaceutical and medical device products from concept to commercialization. Our people’s unique skills and expertise are highly sought by clients seeking the right partner in Australia and have elevated Accelagen to become a CRO of choice.

Accelagen has the capabilities to support clients with the transition of assets from pre-clinical evaluation stage into human clinical trials, defining the development strategy and gathering of key data, required to step through the ethical review landscape. Our highly experienced clinical research professionals, lead all aspects of study conduct, from the design and development, initiation, management and close out of clinical studies, from Phase I to Phase IV. The in-house Accelagen team includes Project Managers, CRA’s and Medical Professionals.

The regulatory team lead the registration processes both in Australia and internationally. This includes new therapeutic products and devices, allowing clients to supply life-saving and critical medicines to patients. Accelagen’s regulatory expertise includes a well-established eCTD dossier publishing service utilizing world leading systems provided through Lorenz.