Menu
Forums
New posts
Search forums
What's new
New posts
All posts
New media
New media comments
Latest activity
Media
New media
New comments
Search media
Resources
Latest reviews
New resources
Search resources
Attachment List
Log in
Register
What's new
Search
Search
Everywhere
Discussion Threads
This forum
Search titles only
By:
New posts
Search forums
Menu
Log in
Register
Forums
Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
JavaScript is disabled. For a better experience, please enable JavaScript in your browser before proceeding.
Other Medical Device Regulations World-Wide
Regulatory systems around the world different from the ones in the above sub-forums.
Prev
1
…
Go to page
Go
48
49
50
51
52
53
Next
First
Prev
50 of 53
Go to page
Go
Next
Last
Filters
Show only:
Loading…
B
Requirements for Exporting Medical Devices to Libya
Burgmeister
Jan 21, 2011
Replies
5
Views
6,854
Jan 24, 2011
Burgmeister
A
Medical Device Registration Fees in Indonesia
Arcadian
Jan 24, 2011
Replies
3
Views
3,576
Jan 24, 2011
Marc
S
Regulatory Requirements for Telehealth or Telemedicine in South Korea
Shayanika
Jan 24, 2011
Replies
1
Views
2,555
Jan 24, 2011
bio_subbu
T
Australia TGA Approval recognized by New Zealand?
tehuff
Dec 28, 2010
Replies
7
Views
4,961
Jan 13, 2011
Adele
Z
Is talking aid device regulated as a medical device in Brazil?
zhang126
Jan 1, 2011
Replies
5
Views
1,992
Jan 11, 2011
zhang126
C
Role and Benefits of PIC/S (Pharmaceutical Inspection Cooperation Scheme)
Cinti
Dec 30, 2010
Replies
2
Views
2,258
Dec 30, 2010
Ajit Basrur
TGA Guidelines on Australian & EU Medical Device Regulatory Requirements Differences
bio_subbu
Jul 31, 2009
Replies
5
Views
3,819
Dec 29, 2010
Mickey1102
E
Any Idea why Manufacturer with CE device does not seek Australian approval?
endlesslovehv
Nov 18, 2010
Replies
7
Views
3,931
Dec 6, 2010
Ronen E
K
Cosmetic Product Registration - South Korea
kp7788
Dec 4, 2010
Replies
1
Views
3,451
Dec 6, 2010
Stijloor
S
Food Grade or USP Class IV Materials for Manufacturing Injectable Products
simon123
Nov 26, 2010
Replies
5
Views
12,669
Nov 30, 2010
Ronen E
E
Conformity Assessment under Australian Medical Device Regulations
endlesslovehv
Nov 21, 2010
Replies
3
Views
2,231
Nov 22, 2010
endlesslovehv
F
Traceability Requirements for Implantable Medical Devices
Frenchuser
Nov 16, 2010
Replies
2
Views
3,626
Nov 19, 2010
Michael Malis
T
FTC "Made In U.S.A" Labeling Rules vs. Saudi Arabia's "Country of Origin" Regulations
tosborn
Nov 18, 2010
Replies
6
Views
7,110
Nov 19, 2010
Michael Malis
E
Medical Device Classes IIa and IIb in EU and Australia
endlesslovehv
Nov 16, 2010
Replies
2
Views
3,518
Nov 18, 2010
endlesslovehv
C
Equipment Purchase Procedure which includes Qualification of Manufacturers
Cinti
Oct 12, 2010
Replies
6
Views
2,857
Oct 14, 2010
bio_subbu
Prev
1
…
Go to page
Go
48
49
50
51
52
53
Next
First
Prev
50 of 53
Go to page
Go
Next
Last
You must log in or register to post here.
Forums
Medical Devices, Medical Information Technology, Medical Software and Health Informatics
Medical Device Related Regulations
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to the use of cookies.
Accept
Learn more…
Top
Bottom