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All the registered users holding valid WHO-GMP certificate are hereby instructed to update their information such as manufacturing license details/ copies, product permission, WHO-GMP certificate & its validity details of products approval/COPPs granted under current certification, contact details and contact person details.


WHO GMP certification Online Application Software has been awarded " SKOCH ORDER OF MERIT" as " India's best e-Governance Project 2014"
ONLINE WHO-GMP SYSTEM

COMMISSSIONER's DESK

New Drug Manufacturing & Sales Website

***Use of Mozilla Firefox Recommended

Guidelines for Issue of SALE License.
Guidelines for Issue of Manufacturing License.
Guidelines for Issue of WHO-GMP Certificate.

Fee structure for WHO-GMP Certificate

:: General Instructions
Manufacturers are requested to read the instructions carefully, before proceeding with the Online System.

I Firstly register yourself. Registration should be done separately for each site e.g: If company "XYZ" has license at Plot no.123, MIDC and Separate license at Plot No.456, MIDC, then you should register separately for each unit.
II Please do not register more than once for the same site. If registered more than once then it will result into incorrect output or results.
III Do not use any special characters such as : , / , \ , ' , " while you enter the name of the licensee. Do not use any prefix such as M/s. etc.
IV For registration of LOAN licensee it is mandatory for complete registration of OWN licensee. After completion of registration of OWN licensee and uploading the relevant information, LOAN licensee will be able to register by selecting the relevant OWN licensee.
V Please follow the instructions displayed on the screen.
VI Please register and enter the authentic and correct data.
VII Please upload all copies of information such as license and its renewal, approved list of products with its renewal copy, site master file, WHO-GMP certificate, COPPs, Process validation reports, stability study reports, BMRs etc in PDF format only.
   
 
   
   

FDA - MAH
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Office of Commissioner, Food and Drug Administration, M.S., Survey No. 341, Bandra-Kurla Complex, 2nd floor, Bandra (East), MUMBAI-400051 .
Tel: +91-22-26592363/64/65 Extn: 2235/2234 E-Mail:whogmp.mahafda@gmail.com