At Benchmark Products, we understand the critical importance of maintaining high standards in cleanrooms and sterile manufacturing environments. Our latest case study showcases a remarkable transformation of a protein manufacturing facility through the adoption of our Suite line of products. Key Highlights Overcoming Environmental Monitoring Challenges: Learn how we helped a facility achieve superior cleanliness…

To achieve the new Annex 1 requirements, life science manufacturers need cleaning and disinfecting solutions that are backed by science and offer reliable, consistent results. In this article, we’ll explore how Suite Ultra-Fiber cleaning and disinfecting solutions can help maintain a sterile manufacturing environment.

The Annex 1 checklist is a helpful tool for life science manufacturers to ensure that their sterile manufacturing facilities are compliant with the latest regulations. With the new Annex 1 guidelines set to take effect in August 2023, it is more important than ever to ensure that your facility is up to date and in compliance.

Not only does mold pose a risk to patient safety, but it can also result in product recalls, financial and reputational damage, and regulatory consequences. However, by using the right preventative cleaning and disinfecting products and procedures, manufacturers can significantly reduce the risk of mold contamination in sterile environments.

Podcast Host Gabrielle Bejarano talked to Chris White, who is the Global Head of GMP at Adamas Consulting, about what’s new and different in Annex 1, and how sterile manufacturing companies and facilities can meet the regulations by the summer of 2023.