Pharmaceutical and agrochemical manufacturers operating within the dynamic, increasingly risk averse regulatory environment look to Pia Pharma as a reliable source of current, accurate regulatory advice when preparing their product development and regulatory strategies. With detailed knowledge of product registration requirements, our experts guide clients through critical decision making stages of development, and support the process with appropriate, individual strategies to meet the desired regulatory goals.

Our regulatory team’s involvement throughout the development of your product is particularly advantageous when preparing the data package to be submitted for approval. It creates a seamless, efficient transition of information from studies into a comprehensive, organised submission to support the integrity of product chemistry, efficacy, safety and trade required in many regulated markets. The good regulatory science presented ensures a registration process with reduced down time associated with additional regulatory requirements or data deficiencies arising from review.

Pia Pharma consults into regulated markets world-wide. We have experience in markets such as New Zealand, south-east Asia, China, South America and the European Union.

Our regulatory affairs experts have the local and international experience that you are looking for.