In the demanding world of pharmaceuticals and life sciences, precision and compliance are critical. Benchmark Products leads the industry by providing high-quality, regulatory-compliant cleanroom solutions. Among those is it’s BioMark Bags™. These single-use bioprocessing bags tailored for the pharmaceutical industry, feature Renolit 9101 film for durability and chemical resistance. The bags have a 5-layer structure, offering…

The Bullard™ Sightline Hood, crafted with Tychem® 2000 material, promises unparalleled comfort and productivity for users in manufacturing suites. Its design boasts features like a sleek profile, a panoramic 320-degree lens, effortless breathing, and a lightweight custom-fit hose that reduces head pressure. Enhanced with a roomy interior, soft sport knit neck cuff, and compatibility…

Benchmark GMP Cleanroom Socks are the ideal solution to keep manufacturing facilities Annex 1 compliant. These socks allow personnel to enter changing rooms leading directly to class B and class C cleanrooms. Additional features include: continuous filament polyester and nylon yarn particulate contamination reduction available in sizes S-2XL

Benchmark Products’ Suite Touchless Mop is used for pharmaceutical manufacturing cleanrooms. It has an ergonomic handle made of anodized aluminum. This adjustable mop handle length ranges from 39″ to 71″ for hard-to-reach areas. It is for use with Suite Ultra-Fiber mop pads.

Benchmark Products’ Suite Ultra-Fiber Wipers are used for pharmaceutical manufacturing cleanrooms. These high-performance wipers are engineered to meet the rigorous standards of cleanliness and durability in pharma and life sciences manufacturing. Available in two sizes, the SC6 and SC12 wipers are designed with a textured pattern to enhance surface cleaning capabilities. They are snag-resistant, non-particulating,…

Benchmark Products’ Suite line of products for pharmaceutical cleanroom offers the Suite Reach Tool with Ultra-Fiber cover. This is the essential tool for hard-to-reach or small spaces and is designed primarily for isolators, biological safety cabinets, RABs, glove boxes and other challenging spaces. The tool is made of stainless steel with an anodized aluminum extension…

Benchmark Products’ Suite line of products for pharmaceutical cleanroom offers the Suite Ultra-Fiber Sponge for cleaning and disinfecting difficult objects and equipment. The core of the sponge is comprised of polyurethane foam for a soft and absorbent surface. The Suite Sponge also has a revolutionary cover of Suite Ultra-Fiber, which is a micro-denier non-particulating fiber…

Benchmark Products’ Suite line of products for pharmaceutical cleanroom offers the Suite SUDS Mop Frame for efficient and sustainable cleaning. It combines the dynamic fiber technology of the Suite Ultra-Fiber mop pads with lightweight and durable design. The gamma-irradiated disposable mop frame eliminates the time and cost associated with cleaning and autoclaving equipment. Made from…

Benchmark Products provides products for critical life science and pharma environments. In this podcast series Exceeding Your Benchmark, they interview leading experts on a variety of trending topics. In celebration of its first year, Exceeding Your Benchmark looks back at interviews with experts from life science and pharmaceutical manufacturing on timely topics from Annex…

In the rapidly evolving domain of life science manufacturing, validation emerges as a cornerstone to ensure that products meet stipulated requirements concerning quality, safety, and efficacy. This pivotal aspect of manufacturing comes to focus as regulatory landscapes shift, mandating stringent compliance to ensure patient safety. In a recent episode of Exceeding Your Benchmark, a…

For an industry where precision and quality control are paramount, pharmaceutical manufacturing is witnessing an evolutionary leap in contamination control practices. Propelled by changes in regulatory environments, such as the EU’s Annex 1 update and ICH Q9 focusing on quality risk management, the sector is shifting from isolated, data-point-centric strategies towards a more holistic…

Contamination control is absolutely critical in the pharmaceutical industry and includes particulate, microbial, product carryover, chemical, and viral aspects of contamination and often involves proactive, reactive, and supporting aspects. However, regulations, liabilities, and patient health added to the mix create data silos that often form multiple processes and make it difficult to create efficient and…

Pharmaceutical companies invest significant resources in research and development to discover new drugs and therapies and improve existing ones. This involves rigorous testing, clinical trials, and obtaining regulatory approval before a drug can be sold. Government agencies, such as the Food and Drug Administration (FDA) in the United States, oversee the approval process and conduct…

In this podcast episode of “Exceeding Your Benchmark,” host Gabrielle is joined by Ashley Harp, Lead Process Engineer at CRB. They discuss the challenges manufacturing facilities like Life Science Companies are facing as they adapt to new technologies and advancements in manufacturing, specifically in the area of combining highly potent active pharmaceutical ingredients (HPAPIs) and…

Between 2022 and 2030, the cell and gene therapy sector is expected to experience a compound annual growth rate (CAGR) of 39.42 percent, BioSpace said of a recent Vision Research Report. This is quite a large anticipated growth; how will startups and current manufacturing companies work to meet this growing demand? On today’s episode of…

Over the summer new GMP Annex 1 regulations were released by the FDA and EMA, prompting new changes to become standard protocolin sterile manufacturing companies. By August 2023, the regulations will take effect and companies will have to ensure that they are in compliance with the guidelines set. Discussing this on a new podcast, host…

Validation and qualification are some of the most critical phases in the lifecycle of equipment and processes within industries like pharmaceuticals and manufacturing. Driven by the necessity to adhere to stringent regulatory standards and ensure high operational efficiency, the distinction between ‘qualification of equipment’ and ‘validation of processes’ becomes paramount. As the landscape of…

Benchmark provides a new bioprocessing solution to maximize efficiency. This is a single-use system for pharma manufacturers for filling, mixing and single-use assemblies.

Commissioning Good Manufacturing Practice (GMP) facilities is a critical yet complex component of the manufacturing sector, especially as facilities grow in sophistication and the standards for quality and safety heighten. Ensuring that clean rooms, HVAC controls, power systems, and other utilities meet stringent requirements is no small feat. Challenges such as permit delays, documentation…

How can life science companies navigate the challenges posed by rapid technological changes and the latest life science regulations, such as the recent EU GMP Annex I regulations for the manufacture of sterile medicinal products? Tom Caffery, CEO of Benchmark Products, highlighted the importance of adapting quality assurance practices and investing in updated facilities…

The stakes for maintaining pristine cleanroom facilities are higher than ever in the pharmaceuticals and manufacturing sectors. Innovations and quality standards in this niche are not just about staying competitive; they’re about setting new benchmarks for excellence and reliability. This is where companies like Benchmark Products come into play, distinguishing themselves through a relentless…

Pharmaceuticals and manufacturing cleanrooms play a pivotal role in ensuring product safety and compliance with industry standards. These controlled environments are critical for the prevention of contamination and for maintaining the integrity of the manufacturing process. However, managing a cleanroom is fraught with challenges, including maintaining stringent cleanliness standards and adapting to the unique…

In the pharmaceutical industry, where the supply chain’s complexity often complicates sustainability efforts, Benchmark Products is emerging as a beacon of environmental responsibility. Through a strategic blend of green packaging, energy-efficient operations, and waste reduction, Benchmark Products not only addresses its ecological footprint but also sets a precedent for the sector. This comprehensive approach…

In an era where supply chain disruptions have become all too common, businesses are striving for solutions that ensure reliability and continuity for their customers. The key to navigating this challenging landscape lies in proactive planning and the implementation of robust supply chain strategies. These strategies not only aim to mitigate disruptions but also…

The intersection of technology and healthcare has ushered in an era of unprecedented innovation, transforming the way chronic and complex conditions are managed and treated. From digital therapeutics offering bespoke management plans for chronic diseases to the groundbreaking potential of RNA-based treatments in gene regulation, the horizon of medical possibilities is expanding. This fusion…

How are AI, IoT, and data analytics transforming the challenges of supply chain management into opportunities for unprecedented efficiency and resilience? On an episode of Expert Insights by Benchmark Products, Daniel Litwin, the Voice of B2B at MarketScale, emphasizes the transformative impact of integrating AI and IoT into supply chains. This integration facilitates data-driven…

The past year has been a landmark period for the pharmaceutical industry, with Benchmark Products at the helm of thought leadership in cleanroom technologies and personal protective equipment (PPE). As we navigate through the complexities of pharmaceutical manufacturing, the insights from Benchmark Products have provided a guiding light for innovations in safety and efficiency….

How is the integration of robotics transforming the pharmaceutical and life sciences industries into more efficient, safe, and innovative fields? Gabrielle Bejarano, representing Benchmark Products, sheds light on the significant impact of robotics and automation technologies, emphasizing their role in enhancing operational efficiency and safety across drug development and manufacturing processes. “The COVID-19 pandemic…

How can lean and just-in-time manufacturing significantly enhance the efficiency and responsiveness of supply chains, particularly in the critical field of life sciences? Wesley Boyce, Professor of Supply Chain Management & Logistics at The University of Nebraska-Lincoln, offers valuable insights into this question, particularly highlighting how these methodologies can drastically reduce lead times, improve…

As the HVAC industry navigates through evolving EPA regulations, Greg Crumpton, VP of Critical Environments and Facilities at Service Logic and host of the Straight Outta Crumpton podcast, sheds light on the significant changes affecting clean room designs and system maintenance. In this episode of Benchmark Products’ Expert Insights series, Crumpton discusses the shift…

On the latest episode of Expert Insights, presented by Benchmark Products, host Jennifer Parker sat down with Greg Steller, National Account Manager for Bullard™, to discuss Bullard’s groundbreaking Sightline product. The Sightline respirator, designed for sterile pharmaceutical manufacturing, offers a 320-degree panoramic viewing lens to ensure maximum visibility and reduce operator claustrophobia. Stellar emphasized…

In this episode of Expert Insights, presented by Benchmark Products, Greg Crumpton, VP at Service Logic and host of the Straight Outta Crumpton podcast, discusses the specialized HVAC requirements for cleanrooms. He explains that, unlike ordinary settings, cleanrooms demand advanced filtration to maintain a controlled environment, preventing contamination and ensuring the integrity of the…

Powered air purifying respirators (PAPRs) are vital in the pharmaceutical industry to ensure worker safety. Greg Stellar, a National Account Manager at Bullard, provides valuable insights into the different types of respirators available, including powered air purifying respirators (PAPRs), for solid dose and cleanroom environments in pharma. Powered air purifying respirators is a cutting-edge…

Aseptic processing is a critical aspect of the pharmaceutical and life science industry, where maintaining sterile and controlled environments is of utmost importance. In our discussion today, we are joined by Matt Ferrin, CFO and COO of Benchmark Products, and Mike Kosinski, President of CEPro, Inc, as they delve into the key aspects of…

In this episode of Expert Insights, presented by Benchmark Products, Greg Crumpton, VP at Service Logic and host of the Straight Outta Crumpton podcast, advises on the frequency of HVAC maintenance. Crumpton suggests following the OEM’s guidance and being especially aware of a company’s operating conditions, geographic location, and ambient weather, as these can…

Particle Shedding in Clean Rooms: In an increasingly cleanliness-obsessed world, it’s becoming evident that choices regarding the materials we use have far-reaching impacts. This is particularly true in highly controlled environments like clean rooms, where the importance of minimizing particle shedding is paramount. The question arises as to whether reusable or single-use garments should…

Flexible isolators are a crucial component in pharmaceutical processing, and Onfab’s Director and Containment Specialist, Mike Brown, offers invaluable insights into their applications. Boasting an impressive repertoire of over 6,500 designs, Onfab caters to diverse processing parameters and GMP classifications, providing comprehensive solutions to meet various requirements. The retrofit isolators offered by Onfab elevate a…

In 2024, Benchmark Products redefined progress with pioneering innovations in life sciences and pharmaceutical manufacturing. At Interphex in New York City, the company showcased its range of life science and pharmaceutical manufacturing products, including the innovative BioMark Bags. These single-use bioprocessing solutions are recognized for their robust durability, chemical resistance, and compliance with FDA standards….

At Benchmark Products, sustainability is at the heart of everything we do. We are committed to providing smart solutions for cleanroom disposable products, ensuring that recycling is performed effectively and responsibly. Our Benchmark GMP and Suite products are designed not only for top performance but also with the environment in mind. Our innovative solutions…

Get a feel for Benchmark Products cleanroom solutions for life sciences manufacturing customers with this mini tour of their facility.

Benchmark Products showcased their line of life science and pharmaceutical manufacturing products during Interphex in New York City April 2024.

In the demanding world of pharmaceuticals and life sciences, precision, and compliance are not just objectives; they are imperatives. Benchmark Products stands at the forefront of this industry, offering a comprehensive suite of cleanroom products and services tailored to meet the specialized needs of these sectors. With a promise of high-quality solutions and a…