At Benchmark Products, we recognize the need to prioritize sustainable practices in all areas of operation. We’re firmly committed to driving significant change in our cleanroom product offerings and how we contribute to a sustainable future. Our Benchmark GMP and Suite products set the standard for high performance, with a strong focus on sustainability. Moreover,…
Cleanroom design and construction are critical elements in the pharmaceutical manufacturing industry to ensure the production of safe and high-quality drugs. In the latest Expert Insights episode, industry experts Matthew Ferrin and Michael Kosinski provide valuable guidance on mastering cleanroom design and planning for future expansion.
We are thrilled to announce the launch of our new Benchmark Sustainability Program, a significant step forward in our commitment to environmental responsibility. At Benchmark Products, we understand the critical role that sustainability plays in the future of our industry, and we’re excited to provide our customers with eco-friendly solutions that support a greener planet….
In pharmaceutical manufacturing, the presence of endotoxin poses a risk to final product quality and patient safety. This article will discuss what endotoxins are, how they can be detected, and how you can prevent contamination.
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.
In this article, we delve into the key points discussed by Mike Brown from ONFAB in an episode of “Expert Insights” focused on HPAPI pharmaceutical manufacturing. Discover how flexible containment solutions, like ONFAB’s isolators, can revolutionize the process and enhance the safety and quality of pharmaceutical products.
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.
Benchmark Products is excited to announce that we will be exhibiting at Interphex 2023 in New York City from April 25-27. We invite you to join us at Booth #2020 to discover our latest technologies and services that can help you become compliant with the new Annex 1 regulations.
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.
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…