Pia Pharma is a one-stop shop for your product development requirements. As the focus shifts from concept to commercialisation, we can guide you through the requirements for data to address any statutory criteria for toxicology, safety, efficacy, trade, occupational health & safety, environmental safety and project manage each to completion. Through strategic partnerships we have with service providers within these fields we can budget, plan, coordinate and execute an array of ‘in-life’ and field studies to produce the required data packages. Our interaction with regulators ensures that we are planning and designing appropriate studies while obtaining the maximum value from your development dollar.
From concept to commercialization, Pia Pharma works alongside your business, compiling data, reports and coordinating submissions to regulators. Each submission is built on good science, something that is recognised and valued by all regulators. Submissions are closely monitored to minimise delays during the evaluation process. Our clients rely on our continual, effective communication with the regulator. We are passionate advocates for your product, arguing good science as needed to tip the scales in your favour. We pride ourselves on minimal delays and a positive outcome for clients from the regulatory evaluation process.
Our clients can take advantage of our seamless transition for post-authorisation compliance testing services. Our laboratories offer an economical option with good turn-around times.