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| medical device Latest News+ XML/RSSBy MediPurpose™ Todd Vecellio Brings More than 10 Years of Sales Experience to MediPurpose By Grey Matter Marketing Santa Barbara, Calif. (May 9, 2013) -- Medical technology firms are increasingly integrating social media/digital strategies into their sales and marketing and product development business strategies. By Kalorama Information The global medical device market reached $331 billion in 2012, just 3% higher than 2011. The healthcare market research firm says reduced growth rate is the result of a challenged healthcare market in Europe and slow funding increases in the U.S. By mVisum Inc. mVisum, Inc. and Airstrip, Inc. announced today that the parties have settled AirStrip’s patent lawsuit against mVisum, Inc. By Visiongain A new report by visiongain predicts that world in vitro diagnostic market revenues overall will reach $81.0bn in 2017. By Therapeutic Monitoring Systems (TMS) Inc. CIMVA Universal - a software platform supporting a range of clinical decision support and diagnostic... By Larada Sciences Professional Lice Device Nearing 3-Year, 50,000 Treatment Milestone Larada Sciences announced today that its LouseBuster™ professional lice device has been used to complete about 50,000 successful head-lice treatments since it first hit the commercial... By Potomac Photonics Stem cells, which have enormous potential in medical research because of their ability to differentiate into specialized cells types, may one day provide a renewable source of replacement cells for people that require organ transplants or are suffering... By MediPurpose™ Clinical Use Studies Also Show 94-Percent Score for Ease-of-Use, Ergonomics and Performance Tests By Global Pacific Manufacturing Group LLC GPMG, a medical device consulting firm, unveiled a quality system product designed for specification developers. The FDA QSR and ISO 13485 compliant system governs all aspects of product development, design transfer, and device master records. By Global Pacific Manufacturing Group LLC GPMG, a medical device consulting firm, unveiled a new product to help Initial Importers of medical devices comply with FDA regulations. The design of the system allows for immediate implementation and fits varying organizational structures. By MediPurpose™ Authorizes Medical Product Company to Continue Distributing babyLance™ Safety Heelsticks and SurgiLance™ Safety Lancets in Canada By MediPurpose Pte. Recertification Validates MediPurpose’s Medical Product Quality Management System (QMS) By Visiongain Visiongain’s analysis: the medical device contract manufacturing market to be worth $119.5bn by 2023. The market generated $33.6bn in 2011, according to Medical Device Contract Manufacturing: World Market Outlook 2013-2023. By MedTech Association AdvaMed and the State Medical Technology Alliance, including MedTech, released a comprehensive policy agenda focused on state-based initiatives that will foster an environment of growth and patient access to the latest in medical innovation. By MediPurpose™ Results From Simulated and Clinical Use Survey at Citrus Valley Medical Center By nContact Innovations In Cardiac Rhythm Management published an article by Dr. H. Edward Garrett, Jr., MD that evaluated nContact’s unipolar epicardial ablation devices, the Numeris® and EPi-Sense® Coagulation Systems with VisiTrax®. By Retectix Retectix, a St. Louis-based medical device company specializing in nanofabricated biomaterials and surgical meshes, won two $1000 grants from the 2012 St. Louis Arch Angels and BioSTL, respectively through StartUp Connection By MediPurpose™ Amware will facilitate U.S. distribution of MediPurpose’s three medical products: babyLance™ infant heel incision devices, SurgiLance™ safety lancets, and MediPlus™ Advanced Wound Care products. By NovaUCD BioInterface 2012, a major international medical device conference by the US-based Surfaces in Biomaterials Foundation starts today at University College Dublin, Ireland and runs until Thursday 25 October. All Press ReleasesBy Sanford Rose Associates - San Diego Denali Allen, CPC joined Sanford Rose Associates® - San Diego team as a Principal in May of 2013. By MediPurpose™ Todd Vecellio Brings More than 10 Years of Sales Experience to MediPurpose By Grey Matter Marketing Santa Barbara, Calif. (May 9, 2013) -- Medical technology firms are increasingly integrating social media/digital strategies into their sales and marketing and product development business strategies. By FlexLeg, LLC Company Takes Reservations of its Prosthetics-Inspired Device Prior to July 15 Launch By Kalorama Information The global medical device market reached $331 billion in 2012, just 3% higher than 2011. The healthcare market research firm says reduced growth rate is the result of a challenged healthcare market in Europe and slow funding increases in the U.S. By mVisum Inc. mVisum, Inc. and Airstrip, Inc. announced today that the parties have settled AirStrip’s patent lawsuit against mVisum, Inc. By Visiongain A new report by visiongain predicts that world in vitro diagnostic market revenues overall will reach $81.0bn in 2017. By LPE Ltd Presenting at Med-Tech Innovation Expo 2013 LPE will be providing an insight into the role of Rapid Prototyping and Rapid Manufacturing within Medical Device... By Larada Sciences A California mom found a way to love lice by turning a lice problem into... By Inteprod Inteprod, Medical Contract Manufacturer, cited for its role as Contract... By Therapeutic Monitoring Systems (TMS) Inc. CIMVA Universal - a software platform supporting a range of clinical decision support and diagnostic... By Larada Sciences Professional Lice Device Nearing 3-Year, 50,000 Treatment Milestone Larada Sciences announced today that its LouseBuster™ professional lice device has been used to complete about 50,000 successful head-lice treatments since it first hit the commercial... By Potomac Photonics Stem cells, which have enormous potential in medical research because of their ability to differentiate into specialized cells types, may one day provide a renewable source of replacement cells for people that require organ transplants or are suffering... By The Jon Block Group The Jon Block Group announced they will be participating in the 2013 annual meeting of the American Academy of Orthopaedic Surgeons, taking place in Chicago from March 19-23, 2013. By Bharat Book Bureau Bharatbook.com Pleased to announce a new report on "In-Vitro Diagnostics Market Analysis to 2017" which gives the business dynamics of major players in the In-Vitro Diagnostics market.. By MediPurpose™ Clinical Use Studies Also Show 94-Percent Score for Ease-of-Use, Ergonomics and Performance Tests By Global Pacific Manufacturing Group LLC GPMG, a medical device consulting firm, unveiled a quality system product designed for specification developers. The FDA QSR and ISO 13485 compliant system governs all aspects of product development, design transfer, and device master records. By Global Pacific Manufacturing Group LLC GPMG, a medical device consulting firm, unveiled a new product to help Initial Importers of medical devices comply with FDA regulations. The design of the system allows for immediate implementation and fits varying organizational structures. By MediPurpose™ Authorizes Medical Product Company to Continue Distributing babyLance™ Safety Heelsticks and SurgiLance™ Safety Lancets in Canada By MediPurpose Pte. Recertification Validates MediPurpose’s Medical Product Quality Management System (QMS) By Visiongain Visiongain’s analysis: the medical device contract manufacturing market to be worth $119.5bn by 2023. The market generated $33.6bn in 2011, according to Medical Device Contract Manufacturing: World Market Outlook 2013-2023. By MedTech Association AdvaMed and the State Medical Technology Alliance, including MedTech, released a comprehensive policy agenda focused on state-based initiatives that will foster an environment of growth and patient access to the latest in medical innovation. By MediPurpose™ Results From Simulated and Clinical Use Survey at Citrus Valley Medical Center By nContact Innovations In Cardiac Rhythm Management published an article by Dr. H. Edward Garrett, Jr., MD that evaluated nContact’s unipolar epicardial ablation devices, the Numeris® and EPi-Sense® Coagulation Systems with VisiTrax®. By Surpass, Inc. Surpass and Surpass-Silicon Valley, LLC (formerly LyChron, LLC) to offer premier preclinical research services, accelerating progress along the product development pipeline. By marcus evans Interview with Cheryl Shea-Frederick, Director, Regulatory Affairs at ArthroCare Corporation By The Jon Block Group Dr. Larry Miller, a Senior Associate at the The Jon Block Group, has accepted an invitation by SPINE Journal to join their Advisory Board. By ComplianceOnline ComplianceOnline, the leading GRC advisory network and former FDA Medical Device Laboratories Deputy Director and co-author of ISO 14971:2000 Dr. Harvey Rudolph will conduct a one and half day seminar on Medical Device Risk Management. By ComplianceOnline ComplianceOnline, the leading GRC advisory network and Robert J. Russell, will conduct a two day seminar on compliance processes for life science products in Brazil, Russia, India and China markets. By Retectix Retectix, a St. Louis-based medical device company specializing in nanofabricated biomaterials and surgical meshes, won two $1000 grants from the 2012 St. Louis Arch Angels and BioSTL, respectively through StartUp Connection By MediPurpose™ Amware will facilitate U.S. distribution of MediPurpose’s three medical products: babyLance™ infant heel incision devices, SurgiLance™ safety lancets, and MediPlus™ Advanced Wound Care products. By NovaUCD BioInterface 2012, a major international medical device conference by the US-based Surfaces in Biomaterials Foundation starts today at University College Dublin, Ireland and runs until Thursday 25 October. Scarp Technologies Selected To Participate in StartUp Chile, Garnering $40k of Equity-Free Seed Capi By Scarp Technologies, LLC Scarp Technologies was one of 101 companies chosen from 1509 applicants to participate in Start-Up Chile, a prestigious business accelerator in Santiago. Scarp gains $40k in equity-free capital, visas, and introductions to the Latin American market. By MediPurpose™ Study Completes Two-Year Redesign Phase, Enabling Launch of New Neonatal Medical Device By American Conference Institute Over 400 life sciences leaders gather in NY in December every year to participate in ACI's Annual Drug & Medical Device Litigation conference, taking place this year for Dec. 3–5, 2012 at the Millennium Broadway hotel in NY. By marcus evans Interview with Tatyana Chorny, Regulatory Affairs, Post-Market Surveillance & Complaints Management at Philips Healthcare By MediPurpose™ Second Singapore Patent Expands International Medical Device Intellectual Property Protection for babyLance By MediPurpose™ Input From Neonatal Nurses Carefully Integrated Into Design Specifications for New Infant Heelstick Device By Med Recall News Prescription Medication Kills Thousands of People Each and Every Year By MediPurpose™ Redesigned Infant Heelstick Device Draws Enthusiasm From Neonatal Nurses By MediPurpose™ New babyLance Heelstick Design Exceeds Benchmarks for Safety, Ergonomics By The Jon Block Group The Jon Block Group announced today that it is engaged in testing new physiological monitoring sensors in optimizing rider performance in motorcycle racing. By SFL Regulatory Affairs & Scientific Communication Shayesteh Fürst-Ladani, Managing Director of the SFL will speak on European Day at the World Medtech Forum in Lucerne, Switzerland. By GPMG Global Pacific Manufacturing Group LLC (www.gpacmfg.com ) has developed an ISO 13485 FDA QSR Compliant Quality Management System By MediPurpose® Joins Kentec Medical and KOL Bio-Medical Instruments as Exclusive Regional Distributors in Western and Eastern United States By SGS Consumer Testing Services IEC 60601-1 3rd Edition requires that manufacturers must address the risks of poor usability, including those associated with identification, marking and documents. By Cambridge Healthtech Institute Aptiv Solutions, Berry Consultants and Tessella announce a one day forum to address the challenges in adopting adaptive trials in the drug, medical device and clinical research industry and assess the potential for transforming drug development. By SGS Consumer Testing Services Along with other applicable standards in the IEC 60601 3rd edition series, IEC 60601-1-11 (2010) outlines new mandatory requirements for the design and verification of a wide range of home use and point of care medical devices. By Bharat Book Bureau Bharatbook.com included a new research report on "In Vitro Diagnostics Market in India 2012" which elaborate profile of the major players in the market along with their financial analysis. By Inteprod LLC Pennsylvania Medical Contract Manufacturer Supports Nationwide Celebration of Manufacturing |
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