Application D for Certificate of Renewal of Good Manufacturing Practices (GMP) to manufacture Ayurveda / Siddha or Unani drugs

Service Details are:

 
Service is defined by the - LINE DEPARTMENT - Directorate of AYUSH(Office of the State Drug Licensing Authority )

The Beneficiary of this service will be Business persons ( G2B )

Types of Service:
Regulatory
(Regulatory Services are those which can be denied by the government)

Do applicant(s) need to register to avail this service?
Yes
The URL at which more information about service are available :
http://eodb.assam.gov.in/
No of Days within which service will be delivered after application submission?
NA          

Note: The time period given is excluding the Government holiday list

Who can apply for this Service?

 
The Application can be submitted by the following:
Institution

How to submit application and Enclosure Details?

  The Application can be submitted by the following:
By Hand
Online
Application can be submitted at the following address:
DISPUR
Pin- 781006
,

Following Documents are required along with the application form

Enclosure Type
Type Of Enclosure Original / Photocopy Attestation Required Documents Recommended
A copy of Form 25 D or 26 D issuing from Drug Licensing Authority Original Not Required A copy of Form 25 D or 26 D issuing from Drug Licensing Authority   
A copy of Previous Form 26 E 1 Original Not Required A copy of Previous Form 26 E 1   
A copy of details of Products Original Not Required A copy of details of Products   
Other Original Not Required Other   



What will Applicant get as Service Deliverable?

  The applicant will receive Output Certificate/Report as the service deliverable(s).
Certificate/Report