The exhibit floor at DeviceTalks West offers ample time for networking with leading industry corporations while discovering the most cutting edge products and services on the market today.
Dedicated Exhibit Hours:
Tuesday, December 11, 2018
10:00 AM – 11:00 AM – Exhibition/Networking Break
12:00 PM – 1:00 PM – Exhibition/Networking Luncheon
4:15 PM – 5:30 PM – Exhibition/Networking Reception
Wednesday, December 12, 2018
10:00 AM – 11:00 AM – Exhibition/Networking Break
11:45 AM – 1:00 PM – Exhibition/Networking Luncheon
The MedTech Conference is your opportunity to connect with thousands of medical technology professionals in one place, at one time. Join us in Philadelphia for business development, innovative technology, and networking with 3,000+ policymakers, business executives and industry leaders.
One of the biggest challenges facing health care providers today is enhancing safety and patient care while managing workflow efficiencies. As a division of the 13th largest global medical device manufacturer, B. Braun Medical Inc. (B.Braun) is uniquely poised to address this challenge. Guided by our Sharing Expertise® philosophy, B.Braun leads the way in developing infusion therapy and pain management products and services that meet the highest standards for quality, safety, sustainability and efficiency.
Boston UX designs compelling touchscreen interfaces for high-impact embedded and connected medical devices. We pair intuitive interface design with expert engineering to create devices both beautiful and buildable.
Helps you meet stringent FDA regulatory requirements
Defines the product features that will appeal to your customers
Applies Design Thinking best practices to create powerful designs
Creates UIs with engaging visual imagery and clever animations
Validates designs with real-world users to gain the insight needed to develop products of superior quality
Boston UX is part of the Integrated Computer Solutions family, a product-driven software company offering development, project management and consulting services.
For over 40 years, Design Standards Corporation has been manufacturing precision medical devices for many of the biggest health care suppliers. We specialize in design and manufacture of disposable and reusable medical devices and instrumentation.
EAG Laboratories, a global scientific services company, offers materials, electronics and chemical testing for medical device development. Surface analysis, polymer chemistry, ISO 10993 Part 18 Chemical Characterization of Materials, failure analysis and litigation support. Nine ISO 17025 laboratories help clients overcome R&D roadblocks, avoid regulatory setbacks, solve problematic manufacturing issues.
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.
General Foundry Service has provided Cast & Machined Aluminum and Zinc Aluminum Components since 1946. For 72 years, “We have poured molten metal into useful shapes in a precise, economical, & timely manner using our Precision Sand, No-Bake Sand, Permanent Mold, Rubber Plaster Molding (RPM) & Investment Casting processes.”
Greenberg Traurig, LLP (GT) has more than 2,000 attorneys in 38 offices in the United States, Latin America, Europe, Asia and the Middle East. GT has been recognized for its philanthropic giving, was named the largest firm in the U.S. by Law360 in 2017, and is among the Top 20 on the 2017 Am Law Global 100. GT’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. Web: www.gtlaw.com Twitter: @GT_Law.
Green Hills Software is the largest independent embedded software provider. With the most safety and security certifications and the best track record for solving embedded problems, Green Hills Software has been leading the embedded world since 1982.
At HealthLink, our mission is to be the number one choice for life science manufacturing companies looking to outsource their logistics and back office services. We achieve this by reducing costs throughout the supply chain and consistently delivering the highest standards in service, quality and efficiency. We are experts in the medical device, diagnostic, human tissue and pharma industry, supporting our clients’ growth in an ever-changing market. Whether you are growing rapidly, changing facilities or switching distribution channels, we seamlessly support your operations throughout the process, in your timeframe.
Medidata is leading the digital transformation of life sciences with the world’s most-used platform for clinical development, commercial and real-world data. Powered by artificial intelligence and delivered by #1 ranked industry experts, the Intelligent Platform for Life Sciences helps pharmaceutical, biotech, medical device companies and academic researchers accelerate value, minimize risk and optimize outcomes. Medidata serves more than 1,000 customers and partners worldwide and empowers more than 100,000 certified users every day to create hope for millions of patients. Discover the future of life sciences.
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.
Minnetronix is a medical technology and innovation company with deep expertise in electronic and electromechanical devices. Founded in 1996, the company creates new technologies and therapies that solve unmet clinical and business needs for patients and medical device companies. Minnetronix is FDA Registered and ISO 13485 Certified.
Promenade provides a full suite of software engineering services for medical devices and instruments. From firmware, device applications, cybersecurity, mobile apps and cloud, we have the expertise to efficiently help take our clients to market with exceptional quality. Our extensive code frameworks and tools facilitate and accelerate the development of your product while offering your engineering teams full control, visibility and accessibility to the instrument internals for development, test, and service.
At Propel, we’re building modern cloud Product Lifecycle 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 PLM software can help.
Qosina is a worldwide supplier of thousands of stock OEM components including bioprocessing accessories, compression fittings, ENFit™ connectors, luers, clamps, clips, check valves, stopcocks, hemostasis valves, tuohy borst adapters, swabs, spikes, syringes and tubing to the medical and pharmaceutical industries. Qosina offers free samples, low minimums and just-in-time delivery. Purchasing from Qosina saves you time and money by eliminating tool costs and providing immediate delivery of in-stock solutions from our ISO 9001, ISO 13485 and ISO 14001 registered facility. Whether you need molded or extruded components, high value plastic or metal, sub-assemblies, tubing or packaging, we can modify any existing component or build new tooling to meet your exact specifications. Contact us or visit qosina.com to view our extensive line.
QuadRite enables Medical device companies to achieve operational excellence while being regulatory compliant by streamlining product engineering and product operation processes. Our simple to deploy and easy to use RitePro™ software is an efficient Design Control, Product Lifecycle Management, Document Management , Quality Management and Training Management solution. It is 21CFR Part 11, Part 820, Euro MDR and ISO 13485:2016 compliant. It has built in Executive Dashboard that provides process metrics and trends to enable continuous improvement.
Medical Device companies that need to bring their electromechanical device to market quickly and efficiently choose RBC Medical Innovations to design and manufacture their products. For over two decades, 7 of the 10 top medical device companies and over a dozen small and mid-size firms, have repeatedly trusted RBC to help them reliably and consistently commercialize their products.
Our clients rely on us to dependably deliver their finished medical device faster than in house development.
RCRI is a leading provider of strategic consulting and integrated clinical trial services to the medical device, IVD, biologics, and combination product industries. For more than a decade, RCRI has been turning medical product concepts into successful, revenue-generating businesses for clients worldwide. More than 450 companies – from entrepreneurial start-ups to Fortune 100 market leaders – have experienced the value of RCRI’s expert insights.
Regulatory and Quality Solutions LLC (R&Q) is the industry leader in providing regulatory and quality consulting and engineering to medical device companies. From strategy to tactical implementation, R&Q partners with clients by providing balanced solutions and hands-on support that enhance the commercialization and post-market processes for medical devices.
For over 25 years, clients have come to Sunrise Labs for complete product development and engineering services, leveraging our ISO 13485:2016 certified process. Specializing in Medical Device and Life Science instrumentation development, we are known for solving tough engineering problems and turning novel ideas into commercially viable products. Our client success stories reflect our strength in software, electronics, systems, mechanical and optical engineering practices.
Our project portfolio includes patient monitoring solutions, neuro, surgical robotics, imaging, cardiac, therapeutic, dermatology, IVD, and connected systems. Located one hour north of Boston, we are proud to employ over 75 dedicated employees in a high-performance culture based on engineering excellence, mutual respect, ethics and integrity.
TASK Micro-Electronics Inc. is a leading microelectronics manufacturing and engineering firm founded in 1987 specializing in the miniaturization, design & manufacturing of custom microelectronic circuits. We take our clients designs and work with them to implement innovative electronic packaging solutions where SWAP (Size, Weight and Power) are important issues.
We service the medical device market in segments such as implantable devices, sensors and endoscopic cameras, just to name a few. We are certified to ISO: 9001-2008 and ISO: 13485-2003 standards.
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.
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.
Velentium offers world class expertise in software, usability, cybersecurity, electrical, and mechanical development for medical devices. Our decades of experience, solid program management and systems engineering will ensure the success of your product.
WuXi AppTec partners with medical device manufacturers, guiding you through the often complicated regulatory process to successfully execute your project. We have supported hundreds of thousands of devices with the strategies and testing needed to gain global market access, avoid costly delays and support changing requirements throughout a product’s lifecycle. Whether your device requires minimal testing or a complex customized program, our team will outline and execute the optimal strategy necessary for regulatory compliance, leveraging decades of accumulated knowledge gained from hands on experience and serving on international standards committees.
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.