In the wake of revised Annex 1 regulations, BenchmarkGMP Cleanroom Socks address the highlighted need for dedicated footwear in Grade B and C cleanrooms. These socks combine compliance with comfort, becoming an essential tool for facilities prioritizing quality and safety.
Benchmark Products is excited to introduce the Sightline Respirator Hood, now available sterile. This innovative product sets new standards in safety, comfort, and vision for pharmaceutical manufacturing.
In this episode of Exceeding Your Benchmark podcast, our host Michelle Dawn Mooney dives into an engaging conversation with Fred Ayers, Advisor for Sterility Assurance for Global Quality Systems at Eli Lilly. Fred imparts valuable insights on the dynamic field of contamination control in pharmaceutical manufacturing.
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.
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.
Breathing Easy: The Best Respirators for HPAPI Cleanroom Environments in the Pharmaceutical Industry
Ensure worker safety in HPAPI cleanroom environments with Bullard’s versatile line of Powered Air Purifying Respirators (PAPRs). Designed for solid dose and clean room settings, these respirators provide effective protection against hazardous substances.
Sheba Zaman of Novatek International is featured on the podcast to discuss how technology can provide visibility and powerful decision making for contamination control in pharmaceutical manufacturing. She explains the difficulties in the industry of digitalizing due to regulations, product safety and taking liability into account. Additionally, she discusses how utilizing data lakes and connecting elements of contamination control can provide insight and trend analysis.
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.
The Exceeding Your Benchmark podcast interviews Jim Fries, the CEO of Rx360, a non-profit that works with pharmaceutical companies and their suppliers worldwide to protect patients from pharmaceutical-related safety issues. Jim explains the Joint Audit Program which is used to assess the quality of manufacturing facilities for pharmaceutical products.
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.