In many industries, manufacturers have reduced development times by using COTS (commercial-off-the-shelf) software and hardware. Pressures to bring new, feature-rich products to market quickly affect medical device manufacturers as much as anyone
Whitepaper: Challenges and opportunities for the medical device industry: Meeting the new IEC 62304 standardOctober 26, 2011 12:25 pm | by IBM
This paper explains what IEC 62304 compliance means for manufacturers. It also describes the larger...
Making Sense of the Major Changes in RoHS for Medical Devices and Monitoring & Control EquipmentAugust 31, 2011 10:54 am | by TUV Rheinland
Significant changes are happening to European environmental regulations. While there has been a...
Wireless technologies are bringing about dramatic improvements in the quality of healthcare by...
Gain best practices in overcoming international labeling challenges at the Medical Device Global Labeling Strategies Conference, July 24-25, 2013 in Minneapolis, MN. This premier marcus evans event will bring together leading medical device labeling professionals to discuss how to successfully create a label on both a national and international scale.
The newly reformatted MD&M East four day conference running alongside the tradeshow, covers everything you need to know from concept development to supplier management, giving you the essential updates to successfully management every step in the product development efficiently and cost effectively.
No longer an "emerging technology," additive manufacturing is leading industry innovation. From design, to prototype to production parts—vision becomes reality at SME’s RAPID Conference and Exposition. This technology has moved beyond ‘plastic’ parts of the past to full scale production in metals, alloys and more. See what’s possible for your operation at RAPID 2013.
Given the number of device applications that involve the transfer of a gas or liquid, it is no wonder pump technology is such a significant part of many healthcare-related products. “Innovation Drives Pump Technology to Meet Today’s Medical Designs” focuses on how today’s medical device demands are being answered by advanced pump technology.
The 2013 Test Center supplement to MDT covers a number of areas of medical device testing relevant to design engineers. One article covers examining and testing the human factor when it comes to the handling of a medical device. Another article focuses on the new ASTM F1929-12 guidelines for testing for seal leaks in porous medical packaging using dye.
Ingestible medical devices offer a convenient, non-invasive method of healthcare; however, the sensitive electronics must be protected. "Coating for Consumption" highlights a coating technology that is being used to guarantee such protection is provided.
The remote patient monitoring field is a rapidly growing one given the advantages it offers for home healthcare, remote regions, and elderly care. However, with it comes a long list of considerations and critical issues for designers and engineers to keep in mind. The cover story examines this area.
AdvaMed 2013 is the leading MedTech conference in North America, bringing more than 1,000 companies together in a uniquely multifaceted environment for business development, capital formation, innovative technology showcasing, world-class educational opportunities and networking.
This paper addresses the capabilities, roles and positioning of systems geared for professional use. Beginning with the most basic information – the definition of 3D printers – this whitepaper positions the two product classes.
The 2012 Medical Molding supplement to MDT highlights several very different aspects of the component fabrication process. Ensuring quality results by establishing effective process monitoring is the subject of one article.
The November/December 2012 cover story, "Industry Forecast," highlights the significant topics for the industry in 2013 and shares the thoughts of leaders from the community. In "Meeting the FDA's Mandates for Unique Device Identification," technology is reviewed that can aid in ensuring manufacturers are in compliance to this coming regulation.
Canada’s manufacturing eyes will be on the newly-improved The International Centre this fall as the country’s national manufacturing event, the Canadian Manufacturing Technology Show (CMTS), returns to the venue after 14 years in downtown Toronto. Asking visitors to “expect more” from the upcoming show—touted the IMTS of Canada—organizers are poised to unveil more details of the dynamic changes to this year’s bigger-and-better event in the months to come.
Scheduled to take place January 28-31 in Santa Clara, Calif., the DesignCon conference program will provide attendees with four full days of intensive technical learning and networking opportunities created by engineers for engineers, and includes 100+ in-depth tutorials, technical paper sessions and panel discussions divided into 14 tracks that address the pervasive nature of signal integrity at all levels of electronic design.
The next staging of HOSPITALAR, 20th International Fair of Products, Equipment, Services and Technology for Hospitals, Laboratories, Pharmacies, Health Clinics and Medical Offices, will take place from May 21 - 24, 2013 at the Expo Center Norte in Sao Paulo, Brazil. At the largest and leading medical trade fair in Latin America, about 1,250 exhibitors from 34 nations will showcase their latest technologies and products to more than 90,000 visitors.
Mediplas is a uniquely focused event for the highly specialized area of manufacturing plastic parts for the medical industry. Mediplas differentiates itself from general plastics shows, as it brings to the forefront the aspects and considerations of medical device manufacturing that do not feature in production for other industries.