Databases of all the registered Medical Devices

C

Chory

#1
Dear all,

I'm new here, and hoping so much that you will help me.

I need links to databases of all the registered Medical Devices (and medicines also, for the matter of fact) of Russia, India, Singapore, Korea, South Africa and more :) Could you direct me to the right sources? I did check the Ministries of Health of those countries, but in most of them there is not much information, or I just couldn't find it...

Thank you very very much!

:)
 
Elsmar Forum Sponsor
C

Chory

#2
Database of all the registered Medical Devices in Japan

Dear all,

I'm looking for a database/lists of all the registered (those who got a license) Medical Devices (and medicines) in Japan.


Is there anything better? :)

Will also appreciate information about the registration process of new/generic drugs in Japan.

Thank you very very much!
 
C

Chory

#3
Databases of Medications and Medical Devices

Hi,

Are there databases of products on the different stages of legalization?

Like, all the products that got IND application approved? Or all the products that have been submitted for IND approval?

Thank you very much!
 
C

Chory

#4
Databases of Medications and Medical Devices

Hi,

Are there databases of products on the different stages of legalization?
And in different countries?


Thank you very much!
 
C

Chory

#5
Database of all the registered Medications and Medical Devices

Hi everyone,

Are there sufficient databases of all the registered medications and medical devices in China? Or those who have been submitted for registration?

Thank you very much!
 

Marc

Hunkered Down for the Duration
Staff member
Admin
#6
Since you are essentially asking the same question in all of these, I have merged your threads into this one.
 
M

michaelrm

#7
The best method I have found is to contact your countries embassy in the target country they normally have a trade representative who's job it is to help facilitate trade and they should be able to inform you of the requirements or at least point you in the correct direction.
 
Thread starter Similar threads Forum Replies Date
M UDI Database and EUDAMED - Will there be two separate databases? EU Medical Device Regulations 3
M CER Adverse events - Justification of databases searched EU Medical Device Regulations 5
Watchcat CERs Literature Databases - Searching for data to evaluate EU Medical Device Regulations 16
P List of ISO certificate registrars around the world - ISO certification databases ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
g_ehs Definition Protocol - for Assertions within Genetic Variant Databases Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 1
M MAUDE & MDR Databases Mismatch Other US Medical Device Regulations 4
J Accessing and Using Databases via a Tablet Device Quality Assurance and Compliance Software Tools and Solutions 4
A Accessing Medical Device Adverse Event databases in EU CE Marking (Conformité Européene) / CB Scheme 7
I Any Recommendations on (M)SDS Databases or Services? Occupational Health & Safety Management Standards 4
A SPC Software Packages - Real Time and can link to Databases including Oracle Statistical Analysis Tools, Techniques and SPC 7
0 Anyone ever worked with the program Rapidminer to datamine databases Reliability Analysis - Predictions, Testing and Standards 4
G Multiple databases that host the same data - TS 16949 database question IATF 16949 - Automotive Quality Systems Standard 6
G Live Tracking & Databases - Are they documents or records? Document Control Systems, Procedures, Forms and Templates 7
Q How to handle the integrity of electronic data in databases? Records and Data - Quality, Legal and Other Evidence 13
M Commercial Quality Assurance Software (ie: SAP) vs. Custom Databases Quality Assurance and Compliance Software Tools and Solutions 12
J Sister-company providing parts is only ISO 9001 registered IATF 16949 - Automotive Quality Systems Standard 7
P Do I need to get registered or have German entity to sell IVD products in Germany? CE Marking (Conformité Européene) / CB Scheme 2
J Searching Registered Medical Devices in Argentina Other Medical Device Regulations World-Wide 0
M Can a PLD Registered in only one state sell prescription drugs to one in another state Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
M DI format for UDI after we have registered it with GS1 Other US Medical Device Regulations 0
Marc Conversations - Limitations for New Registered Members Elsmar Xenforo Forum Software Instructions and Help 8
Marc Old Registered Visitors "Pruned" from the Database - 20180916 Forum News and General Information 0
M Importing a Registered Class II Device, the Applying Our Label - Need New 510(k)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
C First Aid Kit Compliance advice - Registered assembler with the MHRA EU Medical Device Regulations 1
supadrai Establishment registered as specification developer and foreign exporter only 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
Colin Effectiveness of IRCA Registered Training ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 4
S Importer and Registered Place of Business in EU EU Medical Device Regulations 1
M Medical Device Change Requirements - Malaysia Registered Products Other Medical Device Regulations World-Wide 3
Crusader Who is registered to ISO 9001:2015? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 96
Y Is CFDA registration required if the full system is registered by our distributors? China Medical Device Regulations 2
S Change of Medical Device Company Registered Address - Implications Quality Manager and Management Related Issues 3
R Does an Outside Steam Generator need to be Registered in the EU? EU Medical Device Regulations 2
F Fast Track Registration in Costa Rica for Medical Devices registered in Canada Canada Medical Device Regulations 3
X Is in vitro diagnostic instruments not needed to be registered in India ? Other Medical Device Regulations World-Wide 5
O List of ANVISA Registered Companies Other Medical Device Regulations World-Wide 1
I Does my company need to be ISO 13485 registered? ISO 13485:2016 - Medical Device Quality Management Systems 7
S Question on Device Listing for a FDA registered facility US Food and Drug Administration (FDA) 6
Y Solidifier and Spill Kits in US - Why is it registered in EPA not FDA? Other US Medical Device Regulations 6
K Retrospective DHF for an old non-registered device 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
P Other Company's Documentation - Registered as External Documents Document Control Systems, Procedures, Forms and Templates 3
GStough Beating a Dead Horse?....ISO-registered or ISO-certified....THAT Is The Question ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 18
S PAI (Pre Approval inspection) of European non registered site US Food and Drug Administration (FDA) 2
T Requirement for each Company Plant to be AS9100 Registered? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
S Single Warehouse used by two different companies - One is ISO 13485 registered Quality Manager and Management Related Issues 1
B Registered Medical Device Manufacturer - Are documented job descriptions required? ISO 13485:2016 - Medical Device Quality Management Systems 6
M Managing Changes to an SFDA Registered Device China Medical Device Regulations 6
G "Registered Device " and "Listed Device" in TGA Registration for Medical Devices Other Medical Device Regulations World-Wide 4
A Can an EASA approved MRO release (EASA release) a non EASA registered Aircraft? EASA and JAA Aviation Standards and Requirements 2
H Auto Service Repair Shops in Michigan that are ISO 9001 Registered ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
W Listing of ISO 9001 Registered Companies Misc. Quality Assurance and Business Systems Related Topics 4

Similar threads

Top Bottom