KPMG is a global leader in helping organizations across healthcare and life sciences work together in new ways to transform the business of healthcare. KPMG’s Healthcare and Life Sciences practice, with more than 2,800 partners and professionals supported by a global network in 155 countries, offers a market-leading portfolio of tools and services focused on helping our clients comply with regulatory change; improve outcomes through data analytics and advanced technologies; adapt to the consumerization of healthcare; transition to value-based outcomes; and optimize investments to chart their course in a converging healthcare ecosystem.
Emergo by UL is a leading regulatory consulting firm specializing in global medical device and IVD compliance. Our comprehensive solution is designed to help you achieve and maintain regulatory and commercial success. With a presence on six continents, we can provide real-time service and on-the-ground expertise.
Fang Consulting is headquartered in Minnesota’s Medical Alley. Our team of medical device regulatory and quality experts use their knowledge of the US & international regulations to provide premarket and postmarket support to startups and Fortune 500 clients. Our regulatory and quality teams have the experience to ensure our clients obtain the clearances needed to place new products on any desired market and keep existing products on market. We offer customizable on-site and off-site support for regulatory and quality functions.
Assent Compliance is the global leader in supply chain data management. Combining leading-edge technologies with extensive supply chain expertise, Assent provides SaaS solutions that manage third-party data to protect corporate brands, increase market accessibility, and reduce operational and financial risk. Our software suites provide solutions in three categories: product compliance, corporate social responsibility and vendor management.
Castor is a next generation medical device research platform for clinical trials, post-market surveillance (PMS) and post-market clinical follow-up (PMCF). Castor is helping companies efficiently manage patient, medical device and physician data in a centralized platform, decrease time to market and reduce regulatory burdens. Learn more at castoredc.com.
BSI Group Compliance Navigator
As an end to end regulated labeling software company, Innovatum has been a prolific innovator in the life sciences labeling industry for more than 25 years. Innovatum provides fully configurable and validatable labeling software solutions and services including powerful capabilities for MDR/IVDR Eudamed. These systems are easily expandable to meet future regulatory needs without involving the IT department. Additional capabilities include automated 100% print inspection, automated eIFU management and Destination Labeling. Innovatum is ISO 9001:2015 certified.
World Class Label Management Software
PRISYM ID designs and delivers label management software for organizations that need complete product auto-identification and lifecycle traceability. With the continual tightening of labeling regulations and audits, PRISYM ID empowers its clients to safeguard their reputation by ensuring compliance, removing risk and significantly reduce costs by eliminating recalls through labeling errors. PRISYM ID is the market leader in providing validatable world-class label lifecycle management, and is trusted for delivering personalized service excellence to clients.
Covance® and Chiltern, a Covance company, make the drug development business of LabCorp. As the world’s most comprehensive drug development company, we are dedicated to advancing healthcare through a Designed Around You® experience and delivering Solutions Made Real®.
Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, helps our clients identify new approaches and anticipate tomorrow’s challenges as they evolve. Together with our clients, we transform today’s healthcare challenges into tomorrow’s solutions. Information on our solutions can be obtained through our website at www.covance.com.
Empirical Testing Corp
At this time, there are a variety of sponsorship and exhibition opportunities available for companies wishing to increase their visibility and participation in the program, ranging from keynote speaking opportunities through to exhibitor and documentation sponsors. Organizations most suitable for this type of exposure provide services and solutions including:
- European Regulatory Affairs Specialists
- International Regulatory Consultants
- Clinical Research Organizations
- eLabeling & UDI Technology Specialist
- Quality Assurance Software Providers
MedBoard organizes Medical Device information, making it quickly accessible, integrated, actionable and useful, and creates the tools that medical device companies and professionals need. Covering 60+ countries, including regulations, guidance, latest news, standards, definitions, surveillance of market data and much more; all integrated into a unique algorithm and smart search engine which provides relevant results taking the user to the information needed. MedBoard is used by leading organizations and is an essential product for today’s executive.
Eric Jahnke | Sr. Marketing Manager | Q1 Productions
312.955.0424 | email@example.com