FDCA-DMLA
29-Mar-2017 :Wednesday
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Publish DateSubject
12-Apr-2012 test news-2
12-Apr-2012 Test News only for FDL
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
11-Nov-2009 Application Process Workflow Chart
17-Jul-2009 All the Assistant Commissioner and SDI of the Circle offices are hereby instructed that they should start the verification of Phase-I of the fresh loan licence unit ( those who are not having their ow
17-Jul-2009 All Assistant Commissioner and Senior Drug Inspector of Circle offices should ensure manufacturer( OWN & LOAN) under their jurisdiction should complete data entry work of phase- I, II & III by Date –
01-Jul-2009 How to monitor renewals of license & Cancel the license?
30-Jun-2009 How to login & Change Password in DMLA
24-Jun-2009 How to change the firm name
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
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