Our Latest News & Blogs

How GDPR Applies to Medical Devices

With the European Union’s General Data Protection Regulations (GDPR) going into effect May 2018, much of the attention has been on its impact on Internet websites and applications that gather personal information, but it also affects makers of medical devices that offer goods or services to, or monitor the behavior of EU data subjects, according to the EU GDPR organization.

 

 

 

 

 

 

British Researchers Report First 3D Printed Human Corneas

With little fanfare in the media, researchers announced that they had successfully used 3D printing to produce the first human corneas for transplant.

 

 

 

 

Reprocessing medical devices market to grow to $3 billion by 2024

The reprocessed medical devices market will rise from nearly $983 million in 2015 to $3.35 billion by 2024 for a 14.9 percent CAGR according to a report by the market research firm Transparency Market Research (TMP).

 

What You Missed Last Month June Edition

With the beginning of summer, there have also been many updates in the MedTech Industry in the month of June. There has been a 3D printing technique that has the capability of printing biological tissues from multiple tissues, the FDA is now encouraging companies to use electronic systems to move towards a paperless manufacturing process, and the new EU Medical Device Regulation has shown potential to threaten the use of additive manufacturing in medical device creations. Here is a quick recap of what you missed last month:

NSF International offers online learning for MDSAP program

The National Sanitation Foundation (NSF) has produced a series of online training courses for regulatory compliance officers and auditors involved with regulatory processes working in the medical device industry in the five countries participating in Medical Device Single Audit Program (MDSAP).

 

 

Get the latest news and blogs about the Medical Device Industry.

Click 'Subscribe' to keep up with the latest trends.
Image

Kapstone Medical is a single-source service provider to medical device companies lacking the appropriate human capital to bring to market new and safe products. We provide customized solutions that are flexible and cost effective in an ever changing regulatory environment.

 

BBB accredited

Get to Market

Contact Info