Quality
Certificates and licences
Everything your audit and regulatory teams will ask for before the first order, with the reference numbers to check them against.
Drug Manufacturing Licence
Drugs Controller, Himachal Pradesh
NNZ/23/238
Licence held against our works at Plot No. 30, Industrial Area Tahliwal. It covers the manufacture of the coating materials, polymers and resins listed on this site.
Copy on requestWHO-GMP compliance
Assessed against WHO Good Manufacturing Practice
Our unit is operated as a WHO-GMP compliance unit. Manufacturing, cleaning, documentation and release practices follow the same framework your own audit team will be working from.
Copy on requestGST registration
Government of India
02AICPN9961B3ZF
Registered in Himachal Pradesh. Quoted on every invoice.
Copy on requestU.S. Drug Master File
U.S. Food and Drug Administration
Applied. Once filed, the DMF supports customer filings that reference our coating materials, so your regulatory team can cite the file rather than duplicating our data.
Copy on request
Quality and documentation
Do you accommodate customer audits?
Yes. We accommodate customer audits of the Tahliwal works. Write to us with what your quality team needs to see and we will arrange it.
Can we reference your DMF in our filing?
Once the file is issued. The U.S. Drug Master File is applied for, and when it is in place your regulatory team can cite the file rather than duplicating our data in your own submission.
What documentation comes with a supply?
The technical and regulatory documentation your filings need. Tell us what your quality team requires at the enquiry stage so it ships with the material rather than being chased afterwards.
Audits and documentation
We supply the technical and regulatory documentation your filings need, and we accommodate customer audits of the Tahliwal works. Write to [email protected] with what your quality team needs, or start from the contact page.