Concept exploration: A guide to help transition you from MDD to MDR
Michelle Lott, RAC and I believe the medical device industry desperately needs a resource that maps current MDD directives to May 2020 MDR regulations.
It would compare the two so you understand precisely where to focus your efforts.
Would you value it?
It’s too cumbersome – and risky – for us to create on our own. Here’s our dilemma:
The chicken: We would need to spend at least $36,000 to create it.
We calculate we’d need at least 600 hours to compile.
• At $60/hour, that’s a $36,000 expense.
The egg: Is there at least $36,000 in demand for it?
While Michelle and I are willing to spearhead the effort, neither of us can afford to lose money on it.
• Would YOU buy a copy?
• How much would you pay for it?
In sum,
1. The industry needs this resource.
2. We can’t build it ourselves.
3. We can’t afford to risk $36,000.
If you’d value it, now’s the time to indicate your interest.
Please, click below to send me an email.
