Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 99,000 people.
As a leader in global content services, Amplexor provides global governance, compliance, digital experience, and language solutions. Continuously growing since its foundation in 1987, Amplexor has a presence in more than 40 countries and helps customers across key industries, including manufacturing, life sciences, and the public sector achieve process efficiency, increase revenue generation, reduce time-to-market and ensure quality and compliance. Amplexor’s turnkey solutions support core industry processes and include software technology, consulting, system integration, and language and content management services.
From Prototype to Production CGI Motion enables design excellence across a wide range of industrial applications. We thrive on customer driven innovation in precision gearbox, precision machined components and electro-mechanical assembly solutions ranging from aerospace systems to semiconductor applications. We are your design and manufacturing partner helping to differentiate your product, machine or innovation. Our team of problem solving engineers and product managers can bring your application to market on time and under budget. Whether it’s an improvement on a current design or groundbreaking new designs, CGI has the know-how and team to enable design excellence.
With extensive knowledge of the commercialization process, regulatory requirements and scientific trends in the Industry, Eurofins Medical Device Testing offers regulatory compliance expertise and experienced GMP/GLP/ISO 17025 testing to ensure rapid turnaround times with the highest level of service and most advanced technologies for your analytical chemical, microbiological, biocompatibility, electrical, mechanical and package testing needs.
Our scientists and engineers have been assisting companies, large and small, with developmental testing for more than 25 years; and our global network of 16 laboratories in North America, Europe and Asia Pacific provide extensive capacity and the highest level of instrument technology with a full scope of testing services.
Since 1999, Fang Consulting, Ltd. has provided specialized Regulatory Affairs consulting, Quality System consulting, Clinical consulting, as well as device fulfillment, primarily for the medical device industry. Our team is comprised of principal, senior and junior consultants who have a working knowledge of and expertise in the most current global regulations and certifications and work closely with global government agencies. Visit www.fangconsulting.com to learn more about our services.
Greenberg Traurig, LLP has approximately 2100 attorneys in 41 locations in the United States, Latin America, Europe, Asia, and the Middle East. GT has been recognized for its philanthropic giving, diversity, and innovation, and is consistently among the largest firms in the U.S. on the Law360 400 and among the Top 20 on the Am Law Global 100. Greenberg Traurig’s Life Sciences & Medical Technology Group advises clients ranging from start-ups to large multinational public companies to leading research institutions. The group’s attorneys work closely with clients, providing innovative legal counsel to help them achieve their objectives – from discovery through commercialization and product marketing.
Hantel Technologies, located in the heart of Silicon Valley, is a global supplier offering Contract Design and Manufacturing services. Hantel’s team is made up of seasoned professionals that are creative and innovative offering clients a collaborative environment that promotes successful outcomes. Our team regularly tackles a broad range of technologies, with expertise in energy modalities, material selections, intravascular catheters, drug delivery, small instrumentation, and sensors. Hantel offers a full suite of manufacturing services from concept to commercial scale.
During the last 25 years, we’ve reinvented and perfected the stepper motor technology in order to solve problems that had no clear solutions. Today, with our large assortment of standard and custom step motors, linear actuators, BLDC motors, drivers, and controllers, we’re able to provide solutions to even the most unique pains in motion control.
So, if you’re having an issue with your application, then just let us know. Our engineers will eliminate the guesswork. There is no need to buy multiple motors just to find the correct one, because we will configure a motor for your application that will work right the first time!
Created in 1979 by the healthcare technology industry, Medmarc’s purpose is to be the superior provider of liability insurance and related risk management solutions and to support the development, testing and delivery of medical products that save lives and improve the quality of life. Through collaboration with our parent company, ProAssurance, and our clinical trial industry experts, we provide a single source of innovative healthcare liability insurance solutions to the life sciences companies we serve. From ideas and prototypes to the reality of commercialization and success – We can Meet Your Changing Needs. Call me, George Ayd (800) 356-6886, to discuss the cost of insurance coverage, what coverages are needed and when, for your business plan.
At Propel, we’re building modern cloud Product Lifecycle Management, Product Information Management and Quality Management software to help propel your digital transformation. Whether you’re at an established company dealing with potentially more nimble competitors, or you’re ramping a young startup and scaling your business, Propel’s cloud software can help.
Known as the company that brings medical devices to life, Tegra Medical is focused exclusively on the medical device industry, providing end-to-end solutions from prototyping to full production, and from complex components to finished medical devices. Offering a wide range of manufacturing technologies, the company creates devices used in cutting-edge procedures for leading surgical, interventional and orthopaedic companies. Tegra Medical has four locations in the U.S. and Costa Rica and is ISO 13485 and FDA registered and QSR compliant. Tegra Medical is a member of SFS.
Toxikon is a preclinical contract research organization. We contract and partner with biotech, pharmaceutical and medical device industries to deliver exceptional product development services from concept to final product.
Triple Ring believes in standing alongside our clients to solve difficult problems, develop breakthrough products, and create new companies. We work at the intersection of high-tech and life sciences to advance the health and security of humanity and the environment. The team invests in our own work with a solid business sense, strong operational abilities, and a deep technology expertise.
As your co-development partner, we offer our clients access to resources to take projects from concept to customer. Our capabilities span incubation, early R&D, product development, manufacturing, regulatory approval, and market access. Additionally, we have various strategic investment opportunities, including access to our vast innovation ecosystem.
We innovate and manufacture miniaturized and high-precision complex products for our worldwide medical device partners. Our customers are leading suppliers of active implants, medical-grade wearables as well as medical and portable medical equipment. Our activities also cover advanced industrial assemblies, another field where our expertise and sense for innovation are appreciated the world over. For over thirty years, we have helped hundreds of companies develop and produce Class II & III medical devices as well as advanced miniaturized electronic assemblies. Headquartered in Switzerland, our company spreads over three continents with design, development, industrialization and manufacturing sites in Switzerland, the United States and Morocco and employs more than 350 employees worldwide.
Ximedica is a full-service ISO 13485-certified and FDA-registered medical device and diagnostics product development firm. For 30 years Ximedica has provided a unique growth platform enabling organizations to successfully deploy medical technology products into the market. Its headquarters are in Providence, R.I., with offices in Hong Kong, Minneapolis, San Francisco and Silicon Valley. In November of 2014, SV LifeSciences, a Boston-based private equity firm, acquired a majority stake in Ximedica, enabling the company to execute its growth strategy.