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What if the quality of your sterile product depends on something as simple as complex as the way you clean?

Written by Fedegari | Jan 12, 2026 9:19:47 AM

These optimizations contribute to a facility’s ESG objectives while fulfilling Annex 1’s expectation of responsible utility management.
Efficiency is thus not a cost-cutting measure; it is a regulatory virtue, a sign that the process is scientifically understood and continuously improved.


Don’t miss out on this rare opportunity.

Conclusion

In summary, industrial cleaning in the pharmaceutical sector isn’t just a simple preliminary task but a critical scientific discipline to ensure the sterility and safety of final products. The adoption of models like the Sinner’s Circle and the precise balancing of TACT parameters (Time, Action, Chemistry, Temperature) enables companies to optimize their cleaning processes, ensuring not only regulatory compliance but also long-term efficiency and sustainability.
While regulations such as Annex 1 and TR 29 establish guidelines for valid and continuous cleaning, it is essential that companies not only meet compliance requirements but also adopt a scientific approach that allows them to continuously evolve and optimize processes.

Looking ahead, innovation in cleaning process design, real-time monitoring, and the integration of more sustainable solutions will be key to tackling the challenges of modern pharmaceutical production. The adoption of advanced technologies and the intelligent application of the TACT model will further improve efficiency, reducing resource consumption without compromising quality.