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Apply for Manufacture Licence of Cosmetics, Uttar Pradesh
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Fully Online
This portal offers a convenient online platform for applying for a licence to manufacture cosmetics in Uttar Pradesh. Users can submit required documents, complete regulatory formalities, and monitor application progress digitally. The service ensures that cosmetic manufacturers adhere to quality and safety standards as prescribed by the Drugs and Cosmetics Act. By simplifying procedures and enhancing transparency, the portal supports entrepreneurs and industries involved in producing beauty and personal care products across the state.
Apply for Manufacturing Licence of Drugs for Manufacture of Drugs for the Purposes of Examination, Test or Analysis, Uttar Pradesh
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Fully Online
This service allows applicants to obtain a manufacturing licence specifically for producing drugs meant for examination, testing, or analytical purposes. Through the online portal, users can submit applications, upload mandatory documents, pay fees, and track the approval workflow. This facility ensures regulatory compliance while supporting laboratories, research institutions, and manufacturers involved in drug testing. The streamlined digital process promotes transparency, efficiency, and ease of conducting scientific and analytical activities in Uttar Pradesh.
Apply for Manufacturing Licence of Large volume Parenterals/ Sera and Vaccine/ Recombinant DNA derived drugs specified in Schedule C, C(1) excluding those specified in Schedule X, Uttar Pradesh
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Fully Online
This service enables manufacturers to apply for licences to produce specialized biological products such as large-volume parenterals, vaccines, sera, and recombinant DNA-based drugs listed under Schedules C and C(1), excluding Schedule X. The portal provides a streamlined process for documentation, compliance verification, and tracking approvals. It ensures adherence to high safety and quality standards while supporting advanced pharmaceutical and biotechnological manufacturing in Uttar Pradesh.
Apply for Manufacturing Licence of Drugs specified in Schedules C, C(1) and X, Uttar Pradesh
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Fully Online
This portal offers an online facility to apply for manufacturing licences for drugs falling under Schedules C, C(1), and X, which require strict regulatory oversight. Applicants can upload documents, meet safety and quality criteria, and track application progress digitally. By ensuring compliance with stringent norms, the service supports responsible manufacturing and enhances efficiency, transparency, and accountability in the pharmaceutical sector of Uttar Pradesh.
Apply for Manufacturing Licence of Loan Licence for Drugs specified in Schedules C and C (1) excluding those specified in Schedule X, Uttar Pradesh
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Fully Online
This service enables applicants to apply for a loan licence to manufacture Schedule C and C(1) drugs, excluding Schedule X, using another firm’s licensed facilities. The portal simplifies form submission, document uploads, and monitoring of approval stages. It ensures regulatory compliance while supporting businesses that prefer outsourcing production. The system enhances transparency and operational ease for pharmaceutical units operating within Uttar Pradesh.
Apply for Manufacturing Licence of Drugs specified in Schedules C and C (1) excluding those specified in Schedule X, Uttar Pradesh
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Fully Online
Through this portal, manufacturers can apply for licences to produce drugs listed under Schedules C and C(1), excluding those under Schedule X. These drugs often require specific storage and production standards. The system enables online submission, verification, and tracking, ensuring adherence to quality and safety regulations. It supports pharmaceutical manufacturers by offering a streamlined, transparent, and efficient process for obtaining required permissions in Uttar Pradesh.
Apply for Manufacturing Licence of Drugs specified in Schedule X and not specified in Schedules C and C (1), Uttar Pradesh
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Fully Online
This service allows pharmaceutical units to apply for licences to manufacture Schedule X drugs that do not fall under Schedules C and C(1). Schedule X drugs require stringent control due to their potential for misuse. The portal ensures secure digital submission of applications, compliance checks, and progress tracking. It promotes responsible manufacturing by enforcing strict regulatory guidelines while supporting businesses in meeting statutory requirements.
Apply for Manufacturing Licence of Homeopathic Medicines, Uttar Pradesh
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Fully Online
This service enables manufacturers to apply online for licences to produce homeopathic medicines in Uttar Pradesh. The portal simplifies application submission, document verification, and fee payment, ensuring compliance with regulatory standards. It supports manufacturers in setting up or expanding homeopathic production units while maintaining safety and quality norms. Through a streamlined digital process, it enhances efficiency, transparency, and ease of doing business within the homeopathic sector in the state.
Apply for Manufacturing Licence of Repacking Licence for Drugs other than those specified in Schedules C and C (1) excluding those specified in Schedule X, Uttar Pradesh
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Fully Online
This portal provides an online facility for obtaining a repacking licence for drugs not specified under Schedules C and C(1), excluding Schedule X. It allows applicants to legally repack drugs manufactured in bulk into retail-ready packaging. Users can upload required documents, pay fees, and monitor application progress. The service ensures regulatory compliance, supports pharmaceutical businesses, and enhances transparency in obtaining repacking authorizations in Uttar Pradesh.
Apply for Manufacturing Licence of Loan Licence for Drugs other than those specified in Schedules C and C (1) and X, Uttar Pradesh
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Fully Online
This service facilitates applications for loan licences to manufacture drugs not listed under Schedules C, C(1), and X. A loan licence allows applicants to use another licensed manufacturer’s facilities. Through this online portal, users can submit documents, complete regulatory requirements, and track application status efficiently. The system supports ease of doing business by ensuring that pharmaceutical entrepreneurs can outsource production legally while meeting all compliance norms.
