We develop and manufacture quality products with added human value. We are committed to excellence and to continuous improvement.


Our multidisciplinary team, technology and the applied science are the foundations on which we design the quality of our products. This level of quality starts with product definition and development and continues all along the production and life.  

Multidisciplinary Team

We are a team specialized in different academic disciplines. Half of our workforce works in research and development, quality control, production and engineering. We are deeply committed to include and develop young talents by promoting their improvement in technical and interpersonal skills.


Our research and development and quality control laboratories, and the manufacturing plant are equipped with state-of-the-art technologies and operate using the highest standards of quality and efficiency. 


Our manufacturing plant is located at Parque Industrial Pilar, 60 km away from Buenos Aires and required a 14 million dollar investment.  

Situated in a 6 hectare lot and with a 5600 square meter surface area, the plant is equipped with the most advanced technology devoted to the manufacturing of tablets and capsules, specifically to complex products with a high added value for the treatment of HIV-AIDS and neurodegenerative and cardiovascular diseases.

The plant capacity is 100 million tablets and capsules per year. As Laboratorios Richmond continues penetrating new markets, the plant was designed to include new production units and increase its capacity four times. It is equipped with the latest technologies and complies with the international standards required for the manufacturing of pharmaceutical products, following PIC, EMA (European Union) standards and is also ready to certify with the US FDA. The plant was qualified according to quality risk management criteria and has an ISO 9001:2008 certification. To consolidate our international presence, the plant re-certified for good environmental practices according to ISO 9001 and 14001.

In addition to manufacturing drugs, these premises were designed to include areas devoted to the development of new products, preparation of samples for clinical trials and conducting in vitro and in vivo testing. We also perform quality control tasks on all the processes and coordinate the department of Logistics and Distribution.

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