For more than 70 years, Charles River Laboratories, Inc. has evolved into a worldwide support network,allowing us to act as a steadfast partner to our clients, from discovery to lot release testing for accelerating drug discovery and development. The Microbial Solutions division strategically built our portfolio to bring you progressive products and services that deliver accurate,relevant and reliable data to fuel confident decisions on product quality and contamination control. Our unique combination of Endosafe® endotoxin testing, Celsis® rapid microbial detection, and Accugenix® microbial identification and strain typing keeps your manufacturing operations running efficiently and smoothly, lowers your cost to manufacture, and protects your reputation.
At Charles River we continue to kindle the spark that inspired our founding: an urgency to advance human health by supporting our clients’ research every step of the way.
West Pharmaceutical Services, Inc. is a leading provider of innovative, high-quality injectable solutions and services. As a trusted partner to established and emerging drug developers, West helps ensure the safe, effective containment and delivery of lifesaving and life-enhancing medicines for patients. With almost 10,000 team members across 50 sites worldwide, West helps support our customers by delivering over 40 billion components and devices each year.
Headquartered in Exton, Pennsylvania, and in business for nearly a century, West in its fiscal year 2020 generated over $2.147 billion in annual revenue. West is traded on the New York Stock Exchange (NYSE: WST) and is included on the Standard & Poor's 500 index. For more information, visit www.westpharma.com.
Merck, a life science leader, is a business of Merck KGaA, Darmstadt, Germany. Our comprehensive portfolio supports customers during all stages of the drug manufacturing process. With our broad range of products, applications and services including single-use manufacturing, filtration, chromatography and purification, virus reduction, pharma and biopharma raw materials, drug delivery compounds, and engineering and validation services we are committed to best support your goals of intensified, connected or continuous bioprocessing. Our industry expertise and regulatory know-how help you get to clinic faster, allowing you to focus on what matters most — delivering safe, effective therapies sooner to the patients that need them most.
www.merckmillipore.com@companyPTI is a global leader in package quality testing equipment. We specialize in non-destructive testing solutions for high-risk packaging applications in the pharmaceutical and medical device industries. With continuous innovation in the space for new drugs and drug delivery systems, PTI manufactures solutions for container closure integrity, package integrity, and seal quality inspection. Our technologies conform to ASTM and other regulatory standards. PTI offers expertise in container closure integrity test methods for the laboratory and automated solutions for 100% inline production testing.
www.ptiusa.com@companyMicrorite is a USA based GMP consulting and training company with expert services from facility design to product release. Our experts are well published and are involved in industry organizations such as ISO, IEST, PDA, AAMI, ASHRAE, USP and IP as board or expert committee members. Many of our experts have participated in drafting cleanroom, sterilization standards, and more.
www.microrite.com@companyIn the field of Container Closure Integrity Testing (CCIT), OpTek Systems specializes in the provision of positive controls (simulated leaks) used during process validation and equipment qualification. OpTek is a one-stop-shop for all types of positive controls, including laser drilling, capillaries, micropipettes, orifice plates, and wires. Production and services are carried out from our local facilities around the world, in the UK (HQ), US, and Asia.
www.opteksystems.com@companyThe Parenteral Drug Association (PDA) is the leading global provider of science, technology, and regulatory information. The PDA creates awareness and understanding of important issues facing the pharmaceutical and biopharmaceutical community and delivers high-quality, relevant education to the industry. Since its founding in 1946 as a nonprofit organization, PDA has been committed to developing scientifically sound, practical technical information and expertise to advance pharmaceutical/biopharmaceutical manufacturing science and regulation, so members can better serve patients.
www.pda.org/@company