A Decade Strong — Celebrating 10 Years of BMWS
As one of the world’s largest manufacturers of biopharmaceuticals, we leverage our in-depth industry experience for collaborating with top pharma and biotech companies.
Our contract manufacturing business Boehringer Ingelheim BioXcellence™ is built on profound experience in key technologies – mammalian and microbial derived biopharmaceuticals – and supported by a global manufacturing network ranging from US via Europe to Asia that handles the entire production chain, from DNA to aseptic filling. Our track record in commercial and clinical supply is impressive – since initiating contract manufacturing in 1998, we’ve successfully brought 49 biologics to market. Furthermore, we transferred and optimized over 150 development and manufacturing projects focusing on late stage and commercial supply.
We collaborate with partners worldwide, offering capabilities that complement their expertise. Together we turn biologic innovation into commercial success.
ElevateBio is a technology-driven advanced therapy contract development and manufacturing organization (CDMO) powering the creation of life-transforming therapies. The company helps biopharmaceutical partners design, develop, and manufacture therapies from early discovery through commercialization, combining proprietary gene editing technologies and discovery services, cGMP manufacturing capabilities, and industry-leading expertise to accelerate development across a breadth of therapeutic approaches and modalities. Through continuous investment in automation, AI, and next-generation technologies, ElevateBio delivers the quality, speed, and scale partners need to bring advanced therapies to more patients.
Havior is a leading behavioral science consulting firm improving performance in biomanufacturing and other complex, regulated industries. For more than 30 years, we’ve propelled organizations with scientifically-backed approaches that reveal the hidden human drivers behind operational performance, delivering remarkable and measurable results.
Project Farma is an industry leader in providing project management, validation, engineering and consulting services with a proven track record in gene and cell therapy. We partner with gene and cell therapy organizations in addition to healthcare, pharmaceutical, bio-pharmaceutical companies to support finding ground-breaking treatments and solutions. Our gene and cell therapy clients include early stage startups, establish cell and gene therapy companies and CMOs / CROs. We are committed to helping advance cutting-edge medicines by leveraging our deep knowledge and broad experience in cell and gene therapy to meet any new challenges.
ScaleReady is transforming how cell and gene-modified cell therapies (CGTs) are manufactured. Centered on G-Rex® technology, ScaleReady delivers a lean, high-throughput manufacturing platform that is practical, flexible, scalable, and cost-efficient. CGT entities relying on the breadth and scope of ScaleReady’s expertise can expect to save years of time and millions of dollars on the path to CGT commercialization.
Today, G-Rex is used in ~50% of relevant CGT trials and supports 5 commercially approved therapies, including the industry’s most commercially successful cell therapy. The G-Rex Centric™ Platform is the only manufacturing system capable of meeting patient demand and market scale, giving developers a clear path from process development to profitable commercialization.
Vision. Expertise. Success.
AbbVie Contract Manufacturing partners with companies across the globe to develop, scale and manufacture pharmaceutical products and bring them successfully to market.
Drawing on more than four decades of success as the manufacturing division of AbbVie, we have the depth of experience and the technical knowledge to navigate issues and deliver the innovative solutions customers need. We are much more than a CMO – we are your partner for success.
Avid Bioservices (NASDAQ:CDMO), an S&P SmallCap 600 company, is a dedicated contract development and manufacturing organization (CDMO) focused on development and CGMP manufacturing of biologics. The company provides a comprehensive range of process development, CGMP clinical and commercial manufacturing services for the biotechnology and biopharmaceutical industries. With 30 years of experience producing monoclonal antibodies and recombinant proteins, Avid’s services include CGMP clinical and commercial drug substance manufacturing, bulk packaging, release and stability testing and regulatory submissions support. For early-stage programs the company provides a variety of process development activities, including upstream and downstream development and optimization, analytical methods development, testing and characterization. The scope of our services ranges from standalone process development projects to full development and manufacturing programs through commercialization.
We are engineers with deep experience across the product development cycle, from initial ideas to shipping hardware, across industries and specializations, who became frustrated by the cost and complexity of modern manufacturing. So we decided to upgrade it. We started with industrial CT scanning, which for us was the most valuable but underutilized tool in the manufacturing toolbox, enabling us to rapidly inspect essential components non-destructively. But even this industrial advancement felt stuck in the past, using massive, costly hardware, reliant on complicated, outdated software. So we decided to upgrade it. Our company, like our platform, is designed for upgrades. We’re building for greater intelligence, autonomy, and speed.
Our CDMO Services – From Concept to Market As a global leading CDMO, we support your process development and manufacturing needs for biopharmaceuticals. We also support you with the creation of approval documents at an international level. Many years of experience and expertise in finding best-fit solutions, as well as certified quality management and advanced technologies, ensure our high-quality standards. Furthermore, our client-oriented consulting activities, including project management and regulatory support, guarantee your project’s success. With our full-service offering, we are your CDMO partner of choice.
Bluecrux is the leading value chain innovation company, recognized by Gartner™ as one of the world’s top 20 supply chain partners. Our mission is to transform today’s supply chains into the smart, efficient and fully integrated value chains of tomorrow. We do that through our specialized consulting expertise and AI-powered solutions—Axon™ & Binocs™. We work with some of the world’s largest companies—Johnson & Johnson, GSK, Roche, Bridgestone, AkzoNobel, Beiersdorf, Oatly, and more—helping them optimize and future-proof their value chains. Our global presence spans Europe, the US, and APAC, ensuring we’re always close to the action. To discover more, please visit www.bluecrux.com
BIB is a full service CDMO partner offering cGMP and non-GMP mammalian, microbial, gene therapy and cell therapy services.
Cellares is creating the future of cell therapy manufacturing and accelerating access to life-saving cell therapies. The company is developing a one-of-a-kind solution to overcome the limitations associated with manufacturing cell therapies that are more affordable and widely available to patients in need. With Cellares’ proprietary platform—the Cell Shuttle—biopharma companies, academic research centers, and CDMOs will no longer have to compromise by either choosing a manufacturing platform that is semi-automated but lacks workflow flexibility, or one that provides customization but not the end-to-end automation needed to manufacture at scale. The company is headquartered in South San Francisco, Calif.
Körber is an international technology group with about 13,000 employees, more than 100 locations worldwide and a common goal: We turn entrepreneurial thinking into customer success and shape the technological change. At Körber Pharma we are delivering the difference along the pharma value chain with our unique portfolio of integrated solutions
Russell Reynolds Associates is a global search and leadership advisory firm. Our 425+ consultants in 46 offices work with public, private and nonprofit organizations across all industries and regions. We help our clients build teams of transformational leaders who can meet today’s challenges and anticipate the digital, economic and political trends that are reshaping the global business environment. From helping boards with their structure, culture and effectiveness to identifying, assessing and defining the best leadership for organizations – our teams bring their decades of expertise to help clients solve their most complex leadership issues.
APC helps biopharma companies slash drug development times by delivering breakthrough science at lightning-fast process development speed. We thrive on radical collaboration – challenging ourselves and our clients to deliver for patients faster. iAchieve, our proprietary, cloud-based knowledge management platform digitizes every aspect of your medicine’s journey from process definition through process characterization and into the manufacturing facility that best suits your needs.
As a global health care company, Fresenius Kabi is Committed to Life. The company’s products, technologies, and services are used for the therapy and care of patients with critical and chronic conditions. Our Lovo and Cue Cell Processing Systems are designed for their efficiency and scalability with the goal to deliver these cell and gene therapies to patients as quickly and consistently as possible.
Resilience is a technology-focused manufacturing company dedicated to broadening access to complex medicines. Founded in 2020, the company aims to build a sustainable network of high-tech, end-to-end manufacturing solutions to ensure the medicines of today and tomorrow can be made quickly, safely and at scale. By continuously advancing the science of biopharmaceutical manufacturing and development, Resilience seeks to free its partners to focus on the discoveries that improve patients’ lives.
Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Interactive, Technology and Operations services’ all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 674,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.
Asimov is developing a synthetic biology platform – from cells to software – to enable better design and manufacture of next-generation therapeutics. Asimov’s CHO Edge System for biologic production minimizes the risk of cell line development by enabling exploration of vector design space – Asimov routinely achieve titers of 8–11 g/L across modalities.
Asimov is applying the same approach to improve cell & gene therapies – by developing stable lentiviral cell lines and a best-in-class AAV expression system, and enhancing safety profiles through the creation of synthetic tissue specific promoters.
IDA Ireland was founded in 1949 as the Irish Government agency responsible for the attraction and retention of foreign direct investment (FDI) into Ireland. IDA Ireland partners with multinational companies to attract investment, providing jobs for the economic and social benefit of Ireland.
We have partnered with 1,200 companies to establish operations in Ireland, including all the World’s Top 10 Biopharmaceutical companies.
The biopharmaceutical industry has made a capital investment of approximately $10 billion in new facilities in Ireland, most of which has come in the last 10 years. This represents the biggest wave of investment in new biotech facilities anywhere in the world.
Speak with us and you will soon understand why Ireland has developed Europe’s premier biopharma manufacturing cluster.
Repligen is a bioprocessing-focused life sciences company bringing expertise and innovation to our customers since 1981. We are inspiring advances in bioprocessing through the development and commercialization of high-value products and flexible solutions that address critical steps in the production of biologic drugs.
ScaleReady is transforming how cell and gene-modified cell therapies (CGTs) are manufactured. Centered on G-Rex® technology, ScaleReady delivers a lean, high-throughput manufacturing platform that is practical, flexible, scalable, and cost-efficient. CGT entities relying on the breadth and scope of ScaleReady’s expertise can expect to save years of time and millions of dollars on the path to CGT commercialization.
Today, G-Rex is used in ~50% of relevant CGT trials and supports 5 commercially approved therapies, including the industry’s most commercially successful cell therapy. The G-Rex Centric™ Platform is the only manufacturing system capable of meeting patient demand and market scale, giving developers a clear path from process development to profitable commercialization.
The Virginia Economic Development Partnership (VEDP) is the Commonwealth’s lead authority for economic growth, supporting businesses in expansion, relocation, and innovation. At the heart of the Southeast’s second-largest food and beverage processing sector, Virginia offers unmatched access to major metro markets, a skilled workforce, and a robust supply chain. With 43,000 farms, and 160+ warehousing and distribution centers, including extensive cold storage, dozens of packagers and bottlers, Virginia is a strong strategic partner for food and beverage manufacturers. VEDP connects companies with the resources and insights needed to thrive in Virginia’s dynamic business ecosystem. Whether you’re expanding operations or entering the U.S. market, VEDP is your gateway to success.