Benchmark Products

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…

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.

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…

In this episode of Exceeding Your Benchmark, host Michelle Dawn Mooney speaks with Abby Roth, founder of Pure Microbiology, about sterile compounding and contamination control. Abby shares her expertise in microbiology, sterile environments, and best practices in pharmaceutical compounding. The conversation begins with a distinction between traditional drug manufacturing and sterile compounding, highlighting the…

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…

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…

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…

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…

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…

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…

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