How can we help you?
Our industry experience allows us to offer tailored solutions that meet the highest standards of quality and efficiency, supporting our clients every step of the regulatory process.
Before you write to us
We have direct representation in Argentina and a network of partners in Paraguay and Uruguay. We also support market entry processes in Brazil, the United States, and China.
Yes. We work with companies of all sizes: from early-stage biotech startups to multinationals. We also collaborate with research groups, academic institutions, and investment funds.
Timelines vary: an approval for GMO field trials can take between 6 and 18 months, a variety registration between 2 and 5 years. In the initial consultation, we provide an estimate tailored to your case.
Absolutely. We develop economic reports and technological analyses aimed at investors, venture capital funds, and teams needing feasibility studies and market depth insights.
We can do both. Our services are modular: covering the entire regulatory life cycle or specific stages. We also offer on-demand specific services such as reports and partner mapping.