|
|
We provide consultancy for medical device registration, Licensing and approval in India with CDSCO. Visit Medical Device Registration in India consultancy, CDSCO Drug License C (https://www.dknsb.in/)
|
Top Keywords: medical device, medical device registration, device registration, cdsco, consultancy, device, medical, registration, in india, registration in india, registration in, india, medical device registration in, drug license, india consultancy, drug, dknsb, license, for medical, approval, for medical device, regulatory, license consulting, in india with, and approval, approval in, consultancy for, licensing and, india with, licensing, medical devices, devices, ce, consulting, import registration, manufacturing license, Theres a total of 412 keywords.
Inbound and Outbound LinksThere is currently no known inbound links. There is currently no known outbound links. |
Statistics
We first found this page on 2014-01-31 00:00:13 +0000. It was last re-indexed on 2024-09-27 19:47:11 +0000 and with a fetch interval of 90 days it will be fetched again in 4 days on 2024-12-27 or soon thereafter.
Last fetch returned code 200, OK, the current page state is ACTIVE.
Traffic Data for www.dknsb.in
Traffic data is only available for sites with a CashRank of $15 or better, an Alexa rank better than 100,000 or PageRank of 2 or more.If you are the owner of /www.dknsb.in and you want to remove this page from the search results, just use robots.txt
Similar Sites
Consultant for BIS, ISI Mark, EPR certificate, WPC, BEE, CDSCO
Your trusted partner for BIS, ISI Mark, EPR certification, WPC, BEE, and CDSCO consultancy. Call Agile Regulatory Advisor. Get a Free Consultation.
https://www.agileregulatory.com/
- Details - Similar
FDA Registration - FDA Certificate - FDA Agent
FDA registration is the basic requirement for domestic and foreign establishments that manufacture or market food, drug, API, medical devices, or cosmetic products in the USA
https://www.fdahelp.us/
- Details - Similar
21 CFR part 820 - Medical Device GMP
The GMP requirements are described in 21 CFR Part 820, which are similar to international standard ISO 13485
https://www.fdahelp.us/21_CFR_820.html
- Details - Similar
Medical Device Consultants - I3CGLOBAL US INC
I3CGlobal is one of the professional medical device consulting organization that assists customers in obtaining early certifications at a low cost
https://www.i3cglobal.us/
- Details - Similar
More sites similar to Medical Device Registration in India consultancy, CDSCO Drug License C...
Find Another Website
Sponsored Results
Your Ad Here & Hundreds of Other ISEDN Engines & Directories- $3/Month or Less
Your Ad Here & Hundreds of Other ISEDN Engines & Directories- $3/Month or Less