The new area, designed according to European regulations and perfectly integrated into our ISO 13485 certified processes, ensures a controlled contamination environment where materials intended for primary packaging of infusion and injectable solutions are processed.
This allows us to guarantee our partners purity, safety, and maximum compliance with the technical requirements of the pharmaceutical sector.
Thanks to the ISO 8 clean room, we can offer even more flexible, reliable, and continuous production, with rapid response times and high-quality standards—values that have always been at the core of our value proposition.
This initiative is part of the technological improvement path guiding Sifra EST towards a future that is even more competitive and innovation-oriented.