At our Athens site, versatility is our strength. For decades, our team has been a trusted partner in generic drug development. But today, we also help bring some of the most complex pharmaceutical projects to life.
From value-added medicines to high-potent APIs, and from modified release tablets to mini-tablets designed for patient-centric dosing, Athens has the know-how, facilities, and network to take ideas from concept to market.
Expertise that Adapts to Every Project
Our approach is simple: we adapt to the needs of each client and each formulation. A dedicated project manager coordinates with our R&D, analytical, regulatory, and quality teams to ensure that every step, from formulation to dossier submission, is fully aligned with the project’s requirements.
And because Athens operates in full GMP compliance, our clients know their projects are developed to meet the highest global standards.
Our Integration between the Development lab to Manufacturing
One of the biggest advantages of Athens is our integration within the Adragos network. As highlighted in Juan’s article on global manufacturing, we work hand-in-hand with our manufacturing sites and partner CMOs to ensure a smooth technology transfer.
This means that the products we develop in Athens are designed with manufacturing success in mind, minimizing delays, reducing risk, and ensuring a seamless transition from lab to large-scale production.
Innovation Meets Flexibility
Complex projects often come from biotech innovators with groundbreaking ideas but limited manufacturing capacity. Athens steps in to bridge that gap, transforming early-stage molecules into scalable, compliant, and market-ready products.
Whether the goal is entry into the EU market, highly regulated markets like Japan, or global distribution, Athens provides the technical expertise and regulatory support to make it happen.
Your Partner for Any Level of Complexity
From standard generics to innovative drug delivery systems, Athens is here to support every type of formulation challenge.
Our dedicated high-containment facilities enable the safe and efficient handling of high-potent APIs, while our formulation and analytical teams ensure each product is developed under full GMP compliance. Every method we create is designed for a smooth transition into manufacturing, thanks to our close alignment with Adragos’ production network and partner CMOs. This technical integration extends to regulatory pathways as well, where our experienced team supports dossier preparation and submission for diverse global markets, including the EU and Japan.
Whatever the complexity, we will find the solution together.
