Forum

tme3
@tme3
Eminent Member
Joined: Oct 31, 2016
Topics: 0 / Replies: 24
Reply
RE: DHF vs. Tech File/Design Dossier

I believe the DHF to be more valuable than the dossier. I base this off the fact that the DHF is fully auditable by the FDA. Everything from the custo...

8 years ago
Reply
RE: Discussion Topic: Course conclusion and impressions

This course has been very helpful in looking at some of the other areas of the medical device industry that I have not been exposed to. Not only that,...

8 years ago
Reply
RE: Discussion Topic: Your organizational type

Currently, I work for a company that employs the functional organization structure. This helps in allowing all the smaller specialized groups to focus...

8 years ago
Reply
RE: Organization types of medical devices?

Hi, Looking at these different types, the last one in particular stands out to me for certain reasons. First, the fact that the directorate have an in...

8 years ago
Reply
RE: Expense of Regulations

I have to agree with your suggestion of subscribing to a database rather than buying documents one off. This creates a much more sustainable business ...

8 years ago
Reply
RE: Risk analysis in real company

Fortunately I have had the opportunity to sit in on risk analysis session for a new product. The amount of time and effort that goes into creating the...

8 years ago
Reply
RE: What are Design Controls?

An interesting standpoint on design control is that they protect against product liability of design defect. Design defect is concerned with claiming ...

8 years ago
Reply
RE: Important Part of DDP

I think its difficult to pinpoint a single portion of a DDP to be as the most crucial as all portions are critical to a project's success. To answer y...

8 years ago
Reply
RE: Discussion Topic: Supplemental on DHF and DMR

Yes, while a DHF is not needed for an EU release product, design controls are still an integral part of the process and are still integral. While that...

8 years ago
Page 2 / 2