Tanya Mercier

Tanya has over 25 years of invaluable experience in the pharmaceutical industry, predominantly in product development leadership roles, she has a long history of developing products that are tailored to diverse global markets.

Her expertise extends to a comprehensive understanding of CMC requirements, with knowledge and experience in formulation, process development and validation as well as analytical method and specification development and technology transfers. During her time developing parenteral products for global markets, Tanya has worked with contract manufacturing sites and cultivated a profound comprehension of GMP, manufacturing quality and site quality management systems.

Tanya has project management expertise with skills in leadership, communication, time management, problem solving and risk management to support client project requirements.

Tanya’s expertise spans the development of registration applications across multiple key markets, including, Australia, USA, Europe, UK and Asia. Utilising this knowledge and her passion for tackling challenges, she collaborates with clients to develop robust global registration strategies. Her aim is to expedite and optimise the pathway options available whilst and maintaining a dossier that is aligned across all markets as far as practical to minimise lifecycle maintenance challenges.