GOLD DIGITAL INNOVATION PARTNER
Founded in 2006 in New Zealand, Argenta’s talented and committed employees work on a daily basis to deliver excellence in animal health to customers around the world. With research and GMP manufacturing operations in New Zealand, the United States and the United Kingdom, Argenta holds a unique position as the only combined global contract research organization (CRO) and contract manufacturing organization (CMO) dedicated to animal health.
Argenta operates from Molecule to Market in partnership with customers of all sizes from all corners of the world, supporting their research & development, clinical research, regulatory, scale up and manufacturing needs along their veterinary product development journey.
The day-to-day ethos that drives Argenta forward is a mission focused on global partnerships, a Molecule to Market approach, and innovation. At the core of the business and the organisation is collaboration —among the global employee base and with their customers. Working together, Argenta continually challenges the status quo to continuing to innovate to develop the best animal health technologies and products possible.
From animal scientists to veterinarians to engineers and other industry experts, Argenta’s 450+ strong global team is a passionate and diverse group united in their commitment to healthy animals. The company operates from Research & Development locations in New Zealand and the US and (EMA and FDA) GMP approved Manufacturing sites in New Zealand, the United Kingdom (Scotland) and the United States (Fort Dodge, Iowa).
Argenta proudly partners with a vast range of global clients —from small and medium-sized enterprises to the largest industry players. The R&D capabilities and manufacturing facilities scale to service the requirements of the largest multinationals, while, at the other end of the spectrum, Argenta works with startups and small companies by offering capabilities and solutions that help bring their ideas to fruition.
For more information, please visit www.argentaglobal.com.
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The road to an NADA compared to an NDA is shorter, and less costly, but still very challenging and difficult. There are many ways in which the regulatory path in animal health is less risky than in human health, not least because of the ability to do pilot studies in the client-owned animal population. In fact, almost no pivotal clinical studies fail for lack of effectiveness because pilot studies can be done prior to launching the pivotal study. This roundtable will address how to navigate the registration process in animal health, and share tricks of the trade that you need to know to get your product to market quickly.