Accelagen is a full-service CRO focused on clinical trial development and regulatory affairs for the Biopharmaceutical and Medical Device industry. In aligning both areas of product development we maximise the rate of success for products to reach the healthcare market. We assist from early onset of proof of concept through to each trial phase and final market authorisation. Depending on client needs we have the ability to scale up product development via global partnerships across Europe, Asia and the United States. In complementing our clinical services, we provide regulatory strategy planning, eCTD publishing, product lifecycle management and regulatory submissions for the TGA, FDA and EMA. We service local and international clients via our locations across Australia and New Zealand. For further information please visit our website to discover how we may help to develop your products.