DIGITALIZATION OF PHARMA 4.0 OPERATIONS
Implementing digitalization solutions for GMP compliant regulated environments
FOCUSED ON THE PLANT OPERATIONS DIGITALIZATION
At OYTEC, we put the experience and knowledge of our human capital at the service of the client, offering them the best solution to their needs aligned with the business objectives. We do this on 3 pillars that we believe are fundamental:
With the objective to establish a close and lasting Partner relationship with the client based on mutual trust, joint work and excellence in service.
Taking into account human capital as a differential element. The systems have to be designed and developed to help people and encourage their creativity.
Offering solutions on the premise of specialization as the basis of our experience and knowledge. Mainly in GMP compliant regulated environments.
We offer solutions and services oriented to obtain the maximum performance of the customer’s assets and human resources, in order to be as close as possible to the Operational Excellence.
With this we intend to have more productive and efficient assets and resources, managed under sustainability criteria and in accordance with current regulations, guaranteeing the reliability and safety of facilities and people.
EMA and FDA: The 10 Principles of Pharmaceutical AI
The European Union and the United States published the Guiding Principles for Good AI Practices in Drug Development on January 14, 2026, as part of a strategic effort to harmonize regulatory criteria. The EMA-FDA collaborative work initiative has the mission of promoting safety and accountability in the use of Artificial Intelligence with the aim of leveraging data, digitalization, and AI. This work has been analyzed and disseminated by por Guillem López, CSV & QA Manager at OYTEC, author of the article "The 10 Principles of Pharmaceutical AI according to the EMA and FDA". Common...
