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BenchmarkGMP Cleanroom Socks: Aligning with New Annex 1 Regulations

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.
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BenchmarkGMP Cleanroom Socks: Aligning with New Annex 1 Regulations

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.
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Benchmark Products Presents: The New Sightline Sterile Respirator

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.
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[Podcast] Redefining Contamination Control Practices in 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.
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Flexible Containment Solutions for HPAPI Manufacturers: Expert Insights

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.
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Mastering Cleanroom Design: A Blueprint for Future Expansion in Pharmaceutical Manufacturing

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.
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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.
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[Podcast] Connecting Data to Improve Your Contamination Control Strategies

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.
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Discover Cutting-Edge Solutions for Pharmaceutical Manufacturing at Interphex 2023

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.
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[Podcast] Transforming the Audit Process: Innovations in Supplier Evaluations

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.
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Clean and Compliant: Achieving Annex 1 Requirements with Suite Ultra-Fiber Solutions

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.
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[Press Release] Benchmark Products Joins Rx360 to Enhance Quality and Supply Chain Security for Pharmaceutical Manufacturers

Benchmark Products is proud to announce its membership in Rx360, a global consortium of pharmaceutical companies, suppliers, and service providers, dedicated to advancing pharmaceutical supply chain security and quality.
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Get Ready for Annex 1: The Importance of Compliance and How the Annex 1 Checklist Can Help You Get There

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.
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Fighting Fungi: Preventing Mold Contamination in Sterile Manufacturing Facilities

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.
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[Podcast] How Life Science Manufacturers Can Successfully Adapt to Change

In this episode of Exceeding Your Benchmark, Ashley Harp, Lead Process Engineer at CRB, talks about the challenges of pharmaceutical manufacturing adapting to rapid innovation of new therapies and various options to meet demand.
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[Podcast] How Can Cell & Gene Manufacturers Scale to Meet Demand?

In this episode of Exceeding Your Benchmark, Sumit Verma, Senior Vice President Global Strategic Manufacturing at Iovance Biotherapeutics, talks about the challenges faced by new biopharma startups and how cell and gene manufacturers can scale to meet demand.
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[Podcast] What Updated Annex 1 Regulations Mean for Sterile Manufacturing Companies in 2023

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.
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How to Prevent Endotoxin Contamination in Sterile Pharmaceutical Manufacturing

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.
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3 Crucial Factors to Achieve Annex 1 Compliance

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Annex 1: How Will the Revisions Effect Compliance of Your Cleanroom Facilities?

After several years of delays, the EU and FDA are now doubling down on their efforts to force drug manufacturers to comply with Annex 1…
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EU GMP Annex 1: How Will the Revisions Effect Your Cleanroom Facilities?

EU GMP Annex 1 amendments are expected to have a major impact on Life Science manufacturers’ handling and processing of sterilized products in the near future. How can you become Annex 1 ready?

INNOVATIVE SOLUTIONS FOR LIFE SCIENCES' CRITICAL MANUFACTURING ENVIRONMENTS

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