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Publish DateSubject
12-Apr-2012 test news-2
07-Nov-2011 As per DCGI Letter dtd: 23-9-2011 all manufacturers are reguested to limit content of Paracetamol to 325 mg in FDC of Tablet/Capsule & display box warning on label about liver toxicity.
31-Mar-2011 Single Ingredient product permission has become compulsory online from 01/04/2011.
31-Mar-2011 NPPA Survey regarding..please see the attachment : 2 of 2
30-Mar-2011 NPPA Survey regarding..please see the attachment : 1 of 2
21-Feb-2011 Govt. Resolution
03-Dec-2010 Clarification on Additional Product Permission/Additional Brand and Revised Product PErmission
09-Aug-2010 COPP application and attachment regarding
31-Dec-2009 Application Status in iDMLA
01-Jul-2009 How to monitor renewals of license & Cancel the license?
06-Jun-2009 Loanee firm Registration Regarding
04-Jun-2009 Regarding LOAN firm registration and re-print of registration slip
15-May-2009 REVISED PRODUCT PERMISSION-How to apply? and what it is exactly?
06-May-2009 How to enter Kit
20-Mar-2009 Who has to enter LOAN LICENSE details at present?Click this news for details
19-Mar-2009 How to enter loan license details
18-Feb-2009 Regarding COPP Application
03-Feb-2009 Guide Lines to enter Backlog Data of Certificates issued so far to the firm
03-Feb-2009 Standard Operating Procedures(SOP) for Certificates Application
01-Jan-2009 On line application for certificates regarding-Trial basis
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