|
like
comment
share |
< 1 min reading time
There are rumours of potential changes to the FDA approval process particularly geared at devices processed through the 510(k) pathway. Will these changes affect reimbursement strategies? If so, how? Marked as spam
 Posted by Asked on February 10, 2019 5:51 pm
172 views
|
Meet your next client here. Join our medical devices group community.
We still use LinkedIn to access our site because it’s the only way to “pull in” your LinkedIn photo, name, and hyperlink to your profile page, all vital in building your professional network. When you log in using LinkedIn, you are giving LinkedIn your password, not me. I never see nor store your LinkedIn credentials.
