Drug License in Maharashtra
Drug License in Maharashtra
Drugs are one of the most prized yet potent inventions of mankind; the proper utilization of which
hinges on its regulation. In India, drug control is exercised throughout the entire life cycle of the
drug; which involves its manufacture, sale, distribution, and consumption. This article looks at the
requirements and procedure to obtain a drug license in Maharashtra.
Governing Act
India’s drug industry is primarily regulated by the Drugs and Cosmetics Act of 1940 among other
relevant regulations such as the Dangerous Drugs Act of 1930 and other relevant regulations. The
year 1964 marked the inclusion of Ayurvedic and Unani drugs into the former Act, which was until
then kept out of the purview of this provision.
Armband of Execution
The administration of drugs in Maharashtra is vested with the Food and Drug Administration of the
State. The administrative body, which is headquartered in Mumbai, strives to enforce the relevant
Acts in a fair manner by upholding the safety standers and protecting consumers through it.
Infrastructural Specifications
A retail or wholesale operational unit for drugs can be established in a carpet area of 10 square
meters and must include a separate and exclusive entrance. On the other hand, an outlet operated
for both retail and wholesale purposes must be established a carpet area of 15 square meters. In
case of the latter, the area must be legally possessed by the applicant, and again, must include
separate and exclusive entrances.
Interior Specifications
The medical facility must include a refrigerator for the storage of certain vaccinations and medicines.
Apart from this; cupboards, racks and other pertinent utilities are required for the storage of drugs.
Appointment of Personnel
The operations of a retail medical store can be entrusted to a registered pharmacist. A wholesale
store owner may either avail the services of a competent person holding a graduate degree with
more than a year of experience in the procurement and sale of drugs or a Registered Pharmacist.
Fee Requirements
Retail Chemist Shop Licenses for sale of Allopathic and Homeopathic medicines can be availed by
remitting a fee of Rs. 3250.
Wholesale shop licenses (whether a fresh one or the renewal of an existing one) can be availed by
remitting a Fee of Rs 3000.
Wholesale shops specifically dealing with Homeopathic medicines requires a remittance fee of Rs.
250 so as to be licensed.
Retail sale of Schedule X drugs can be pursued by paying a fee of Rs. 600. Wholesale outlets are
required to remit a sum Rs. 1200 to avail the same provision.
Documents Required
Let us understand the documentary requirements for various licenses issued under the umbrella of
trade license:
Application form in Form 19 (for Retail license), Form 21 (for Wholesale License), Form 19B (For
Retail Homeopathic license), Form 20C (for Wholesale Homeopathic License), Form 19C (for Retail
and Wholesale license of Schedule X Drugs), and Form 19A (for Retail Restricted license). For the
awareness of the applicants, these forms need not be signed by all partners given its statutory
nature.
Scanned PDF of the partnership deed and the receipt of the Registration fee paid to the Registrar
of Companies (for partnership firms).
No Objection Certificate (for Societies, residential premises leased by CIDCO, MHADA or similar
Government/Semi Government Agencies).
Change in Premises
Rental/lease agreement.
Documents of the Registered Pharmacist (if a wholesaler is applying for retail license).
Certificate of Registration.
24 hours open application – only with three pharmacists and safety measures.
Surrender of License
Change in Director
No Conviction Certificate
Copy of tender.
Application Procedure
As we have now covered the fundamentals, let us analyze the procedure to apply for this vital
document:
The applicant may initiate the proceedings by visiting the official website meant for this purpose.
The option “New login ID and PWD” (which is found on the right-hand side of the webpage) must be
opted for. Choose the option ’MH’ from the drop-down menu.
In the following page, the user will be presented with two options, among which the first one is
meant for existing license holders and the latter for new applicants. Choosing any of the options will
direct the applicant to a page for specification of information, which must be duly filled and saved.
The User ID and Password will be delivered to the registered mobile number of the user within 24
hours.
Step 4: Login
The user may log in to the portal by entering his/her username and password.
Choose the option ‘prepare/edit online application’, which can be found in the left-hand corner of
the page.
Click on the ‘Inward button’ found on the page and opt for the desired ‘Inward type’.
The user is required to take a print out of the application and duly sign the same.
The required documents must be uploaded, after which the user will be directed to the payment
gateway.
Step 11: Remittance of Fees
Upon the completion of the inward application procedure, the applicant would be necessitated to
remit payments. This can be done through the ‘makepayment’ tab which appears after the process
of inward application is done with. Clicking on this will take the user to the ‘make a new payment’
tab,’ thereby redirecting the user to the ‘Gras’ site of the Government of Maharashtra.
The applicant will now be asked to make his/her choices, the likes of which include:
Department (the option Food and Drugs Administration is apt for this purpose).
Payment types (choose the category for which the payment is to be made); e.g. – drug sale
license.
Scheme name
District of enrollment.
Form ID.
Options of payment.
The payment can be remitted based on the module chosen by the applicant, courtesy the GRAS
website.
After the payment is deposited through the GRAS System, a payment receipt may be printed and
uploaded in the system, post which the application can be forwarded to the department.
This concludes the application process. The concerned authorities will review the application upon
receiving it. Queries are raised by the inspector and/or Licensing authority or Assistant
Commissioner for incomplete and inadequate submissions. If unsatisfied with the response of the
applicant, the certificate will be reverted back to him/her so as to resubmit the same by making the
necessary changes.
It intimates/substitutes another drug in a manner that the name of such drug is identical to that of
another except if it’s plainly and conspicuously marked to reveal its true character and its lack of
identity with the latter.
The label of the container of the drug is identical to the name of an individual or company claiming
to be the manufacturer of the drug, the likes of which is fictions or non-existent.
It purports to be the product of a manufacturer who holds no ownership rights for the same.