Question
As originally asked by
In the past year, I’ve seen something that I haven’t seen in my whole career of medical device compliance work. Devices that don’t work (software and hardware problems), serious compliance issues with performance (especially requirements from particu...
source: https://www.linkedin.com/groups/78665/78665-6032178835502485505
The number of medical apps grows by the day, also the capability of such apps continues to improve. With the internet being effectively border-less, is it inevitable, that the regulatory bodies will not be able to control or regulate a significant po...
While market research firms are drafting their predictions of what medical device trends to expect for next year, I thought it would be an interesting time to get some feedback from medical device professionals directly. I'll share a few things I've ...
The article does not seem to make it clear, but the "stem cells" are not from the same patient, but mesenchymal stromal cells from someone else's bone marrow and transiently expressing a notch1 intracellular domain. See more on the SB623 support cell...
Come September 24, 2015, all medical device manufacturers of Implants, life-sustaining, and life-supporting devices marketed in the U.S. need to submit unique device identifiers to the FDA. It's complex, so please accept this free help from my friend...
A perennial sales and marketing problem. Here's one way to address it. How Should Content Marketing Impact Your Selling?How Should Content Marketing Impact Your Selling? by Douglas Karr on Marketing Technology Blogsource: https://www.linkedin.com/gro...
This will be interesting for marketers, sales people, and business development group members. Two years back I showed my client 33 screen shots from relevant sites to determine the best direction for his new website. (I made a 12-minute video about t...
As originally asked by
