A bill that would permit third parties to repair a range of electronic products and have access to diagnostic information as well as OEM-sanctioned parts, is the subject of a hearing on Beacon Hill on September 26. The bill, … Read the rest
Toledo, Ohio – NAMSA, the world’s only Medical Research Organization (MRO) that accelerates medical device development through integrated laboratory, clinical and consulting services, announced today that it has been recognized for excellence in clinical research and honored as a … Read the rest
ALISO VIEJO, Calif. – OCTANe, Orange County’s life science and technology accelerator organization, and MassMEDIC, a regional medical device cluster group, today announced that they have an … Read the rest
(originally published in the DeviceTalk blog on March 9, 2016)
Manufacturers in the healthcare industry are facing a mix of cost and pricing pressures, from government regulations to changes in how … Read the rest
The Art of Designing for Infection Prevention
By Lise Moloney, director of business development, healthcare, Sciessent
We’ve all read the horror stories about healthcare-associated infections (HAIs) wreaking havoc at hospitals across the U.S. and the globe. Many HAIs, including … Read the rest
UDI: If You Do It, Will They Use It?
By Karen Conway, Executive Director, Industry Relations, GHX
We are about the cross the second major milestone for healthcare manufacturers when it comes to compliance with the US FDA’s Unique Device … Read the rest
WHAT IS THE PROCESS TO GET MEDICAL DEVICES REIMBURSED IN CHINA?
By Ames Gross, Pacific Bridge Medical
Getting medical devices registered and approved in China has become much more difficult with the October, 2014 reforms. The cost is higher … Read the rest