| Title | Type | Source | Release Date | Scraped | Download | Status |
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Form27C.pdf
▶ Summary
This document is an application form (Form 27-C) for the grant or renewal of a license to operate a blood bank for processing whole blood or preparing blood components. It outlines details required from the applicant, such as the names of medical staff and premises details. The application must be accompanied by various supporting documents and a copy sent to specific regulatory authorities.
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document |
Gujarat FDA - News Feed
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Dec 12, 2025
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Form27B.pdf
▶ Summary
This is a general document, Form 27-B, for the application to distribute drugs specified in Schedules C, C(1), and X under the Drugs and Cosmetics Rules, 1945. It details the necessary licensing requirements, including details about the expert staff and premises where drugs will be manufactured and tested. A fee structure and the submission of a premises plan are also mentioned as part of the application process.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form27A.pdf
▶ Summary
This document is Form 27-A related to the application for a loan license to manufacture drugs specified in Schedules C and C(1) of the Drugs and Cosmetics Rules, 1945. It covers requirements such as details of expert staff, agreements with the manufacturing concern, and other procedural formalities for the application. The document includes a date of GSR amendment as 27.10.2017.
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Gujarat FDA - News Feed
Unknown
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Dec 12, 2025
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Form27.pdf
▶ Summary
This document appears to be a form (Form 27) related to the application process for obtaining a license to manufacture certain drugs under the Drugs and Cosmetics Rules, 1945. It includes details such as the location of the manufacturing premises and the qualifications of the staff responsible for manufacturing and testing the drugs. The document also mentions fees related to the licensing process.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form24F.pdf
▶ Summary
This document appears to be an application form (FORM 24-F) for the grant of a license to manufacture drugs specified under Schedule X of the Drugs and Cosmetics Rules, 1945. It includes sections to provide details of the drugs, technical staff qualifications, and fee payment information. The document may include notes related to amendments as indicated by references to omitted sections and specific governmental notifications.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form24C.pdf
▶ Summary
The document is an application form (Form 24-C) for a license to manufacture or distribute homoeopathic medicines. It includes sections for the applicant's details, the homoeopathic preparations to be manufactured, and the technical qualifications of the staff. The form references Rule 85-B and includes fields for submission details like the fee payment and premises plan.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form24B.pdf
▶ Summary
This document is an application form for a license to repack drugs, excluding certain specified ones, under Form 24-B as per Rule 69. It includes sections for applicant's details, drugs to be repacked, qualifications of competent staff, and fee payment information. The form must be submitted with a premises plan, but no specific release date is mentioned.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form24A.pdf
▶ Summary
This document appears to be an application form (Form 24-A) related to the manufacture and distribution of drugs under the Drugs and Cosmetics Rules, 1945. It includes sections on the description of drugs, information about the expert staff, enclosed documentation, and fee payment details. The document is not a direct advisory or notification but rather a procedural form likely used by applicants in the pharmaceutical industry.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form24.pdf
▶ Summary
This document is a formal application form (Form-24) for obtaining or renewing a license to manufacture or distribute drugs in compliance with the Drugs and Cosmetics Rules, 1945. It requires details like the names of drugs, qualifications of technical staff, and includes a note about submission accompanying a plan of the premises. The document appears to be a generic application form relevant to regulatory affairs in drug manufacturing.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form19B.pdf
▶ Summary
This document is a Form 19-B application for a license to sell, stock, or distribute Homoeopathic Medicines either by wholesale or retail. It requires applicants to provide details such as the location of business premises and the competent person supervising the sale of these medicines. The form involves a payment of a specific fee to the government for processing.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form19AA.pdf
▶ Summary
This document appears to be an application form for obtaining a license to sell, stock, or distribute drugs from a motor vehicle. It involves filling in personal or business details, drug categories, and vehicle registration number required under the applicable regulatory framework. It includes sections on required fees and storage accommodations related to the application process.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form19A.pdf
▶ Summary
This document is an application form (Form 19-A) for obtaining a restricted license to sell, stock, or distribute certain drugs without a qualified person's supervision, under the Drugs and Cosmetics Rules. The form outlines the conditions under which drugs can be sold and the requirements for storage and purchase. It also specifies fee details and is issued as per rules applicable to drug dealers.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Form19.pdf
▶ Summary
This document is a form used for applying for a license to sell, stock, exhibit, or distribute drugs in India, excluding those drugs specified in Schedule X of the Drugs and Cosmetics Rules, 1945. It includes sections for applicant details, categories of drugs to be sold, supervision requirements, and a fee section. The form's applicability and sections to be filled depend on the type of drug distribution being undertaken.
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Gujarat FDA - News Feed
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Dec 12, 2025
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procedures.pdf
▶ Summary
This document appears to be an internal communication or report from the 'Drugs Control Organisation' regarding structure and processes related to drug control and other internal directives, dated 2015. It covers various procedural aspects and references to legal acts and regulations, but there is no clear external audience or intended public communication. The document is heavily formatted with technical and legal terminologies, suggesting it could be part of an internal or specialized report.
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document |
Gujarat FDA - News Feed
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Dec 12, 2025
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all_forms.pdf
▶ Summary
The document comprises forms and procedural details related to drug testing, analysis, and licensing under the Central Drugs Standard Control Organization, Ministry of Health and Family Welfare, Government of India. It includes templates for memorandums to the Central Drugs Laboratory for testing drug samples and applications for importing drugs excluding those specified in Schedule X. The forms indicate procedures and requirements for regulatory compliance with the Drugs and Cosmetics Act, 1940.
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Gujarat FDA - News Feed
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The%20Juvenile%20Justice%20%28Care%20and%20Protection%20of%20Children%29%20Act,%...
▶ Summary
This is a legislative document from the Ministry of Law and Justice in India, detailing The Juvenile Justice (Care and Protection of Children) Act, 2015. The document outlines amendments and comprehensive provisions for the care, protection, rehabilitation, and legal rights of children in conflict with the law and in need of protection. It provides definitions and scope of application of various terms and procedures under the act, aiming to ensure children's rights and welfare.
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Gujarat FDA - News Feed
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Dec 12, 2025
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E_455_2011_009.pdf
▶ Summary
This document appears to be an excerpt from the Gazette of India published on May 5, 2006, containing regulatory orders or amendments. It includes detailed legal or regulatory language that pertains to modifications in existing rules under a specified Act. The document is of an official nature and resembles government orders or directives, signed off with references to specific parts and sections of the legal framework.
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order |
Gujarat FDA - News Feed
Unknown
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Dec 12, 2025
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pdf ↓ | ✓ Relevant |
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1_10_1_patents-amendments-rules-2005.pdf
▶ Summary
This document is a public notice issued by the Ministry of Commerce and Industry, Department of Industrial Policy and Promotion. It details amendments to the Patents Rules, 2003, following updates to the Patents Act, 1970, to omit certain figures and letters and make provisions for how applications should be filed. The notice specifies procedural changes and requirements for patent filings and amendments.
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public notice |
Gujarat FDA - News Feed
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Dec 12, 2025
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1_69_1_patent_2005.pdf
▶ Summary
This document is the Patents (Amendment) Act, 2005, which received assent from the President of India and is meant to modify the existing Patents Act of 1970. It includes detailed amendments to various sections of the original Act, outlining changes in procedures and definitions related to patents. The adjustments aim to align with international agreements like the Budapest Treaty and the Patent Cooperation Treaty.
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Gujarat FDA - News Feed
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Dec 12, 2025
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E_906_2013_011.pdf
▶ Summary
This document is an official gazette notification from the Government of India, issued on April 23, 2013, containing amendments to the Patent Rules, 2003. It details procedural changes and stipulations for filing applications and maintaining records related to patents. The document is primarily targeted at entities involved in patent filing and administration.
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order |
Gujarat FDA - News Feed
Unknown
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Dec 12, 2025
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pdf ↓ | ✓ Relevant |
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158976.pdf
▶ Summary
This document is an official government notification issued by the Ministry of Commerce and Industry regarding amendments to the patent regulations. It details modifications to the Patent (Amendment) Rules, 2014, including procedural changes related to the filing of patents. The document invites public comments and suggestions for these rule changes.
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order |
Gujarat FDA - News Feed
Unknown
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Dec 12, 2025
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pdf ↓ | ✓ Relevant |
| Unclassified |
Gujarat FDA - News Feed
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Dec 12, 2025
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1_31_1_patent-act-1970-11march2015.pdf
▶ Summary
This document is the text of The Patents Act, 1970, a legal Act enacted by the Parliament of India to amend and consolidate laws related to patents. It includes definitions, interpretations, and detailed chapters covering various aspects of patent laws in India such as application, examination, and rights conferred by patents. The document serves as a comprehensive guide to the framework and provisions of Indian patent law.
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document |
Gujarat FDA - News Feed
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Dec 12, 2025
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RTI_Act.pdf
▶ Summary
This document is the publication of The Right to Information Act, 2005 by the Ministry of Law and Justice, New Delhi. It outlines the framework for public access to information from government authorities to promote transparency and accountability. The document details definitions, scope, and the obligations of public authorities under this Act.
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document |
Gujarat FDA - News Feed
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Dec 12, 2025
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Pre-Conception-And-Pre-Natal-Diagnostic-Techniques-Rules-1996.pdf
▶ Summary
This document discusses the rules and regulations under the Pre-Conception and Pre-Natal Diagnostic Techniques (Prohibition of Sex Selection) Act, 1994, including the specifications for genetic counseling centers, laboratories, clinics, and the sale and use of related equipment. It outlines qualifications for employees, equipment requirements, and legal guidelines for preventing the misuse of diagnostic techniques for sex selection. These comprehensive rules aim to regulate and prevent the misuse of prenatal diagnostic techniques.
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document |
Gujarat FDA - News Feed
Unknown
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Dec 12, 2025
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pdf ↓ | ✓ Relevant |
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pre-conception-pre-natal-diagnostic-techniques-act-1994.pdf
▶ Summary
This document comprises the Pre-Natal Diagnostic Techniques (Regulation and Prevention of Misuse) Act, 1994 and its amendments. It outlines regulations to prohibit sex selection and to govern pre-natal diagnostic techniques for detecting genetic abnormalities. The document details definitions, regulations, and prohibitions imposed by the Act to prevent misuse and enforce compliance.
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Gujarat FDA - News Feed
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Dec 12, 2025
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food%20safety%20and%20standards%20Act%202006.pdf
▶ Summary
This document is the Food Safety and Standards Act, 2006, which outlines the establishment of the Food Safety and Standards Authority of India, its composition, functions, and powers. It consolidates the laws related to food safety in India, stipulating standards for food articles to ensure they are safe for consumption. The act also describes the responsibilities of food business operators, the penalties for non-compliance, and the procedures for enforcement and adjudication.
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document |
Gujarat FDA - News Feed
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Dec 12, 2025
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GSR%2063%20dtd%2016.3.15.pdf
▶ Summary
This document is a notification issued by the Department of Health and Family Welfare of the State Government of Rajasthan. It announces amendments to the Rajasthan Clinical Establishment (Registration and Regulation) Rules, 2013, including changes in rules regarding registration, rule modifications, and fee payments. The amendments come into effect immediately as of March 16, 2015.
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order |
Gujarat FDA - News Feed
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Dec 12, 2025
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GSR%2016%20dtd%206.6.13.pdf
▶ Summary
This document is an official notification from the Government of Rajasthan regarding the constitution of the District Registering Authority under the Clinical Establishment (Registration and Regulation) Act, 2010. It details the roles and members involved, including the District Collector and Chief Medical & Health Officer. This is issued by the Deputy Secretary of the government.
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order |
Gujarat FDA - News Feed
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Dec 12, 2025
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Bill102021.pdf
▶ Summary
The document is a legislative bill titled 'THE CRIMINAL LAWS (RAJASTHAN AMENDMENT) BILL, 2021', proposed to amend sections of the Indian Penal Code, 1860, and the Code of Criminal Procedure, 1973, specifically related to the adulteration of food, beverages, and drugs. Notably, it proposes increased penalties for such adulteration if it is found to be dangerous to human life. It is intended to be enacted by the Rajasthan State Legislature and will come into effect on a date specified by the government in the Official Gazette.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Bill212022.pdf
▶ Summary
This document is a legislative bill from the Rajasthan government titled 'Right to Health Bill, 2022'. It outlines the provisions and definitions related to the right to health, emergency medical treatment, and public health services for the residents of Rajasthan. The bill aims to ensure access to healthcare and protect the health rights of individuals within the state.
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Gujarat FDA - News Feed
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Dec 12, 2025
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169511.pdf
▶ Summary
This document is the Repealing and Amending Act, 2016, issued by the Ministry of Law and Justice in India, published in The Gazette of India Extraordinary. It outlines the repeal and amendment of various enactments as specified in its schedules, without affecting the validity or established legal principles of any acts already done under the repealed enactments.
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document |
Gujarat FDA - News Feed
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Dec 12, 2025
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Act%2026%20of%202008.pdf
▶ Summary
This document is an official publication from the Indian government detailing amendments to the Drugs and Cosmetics Act, 1940. It outlines new regulations and penalties for adulterated or spurious drugs and cosmetics to ensure public health safety. The amendments establish stricter controls and penalties for violations, introduced after receiving the President's assent.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Bill%20No.%20LVIII%20of%202013.pdf
▶ Summary
This document is a Bill introduced in the Rajya Sabha to amend the Drugs and Cosmetics Act of 1940. The amendments aim to regulate drugs, cosmetics, and medical devices with a focus on safety, efficacy, quality, and conduct of clinical trials. The Bill details specific changes like substituting 'Inspector' with 'Drugs Control Officer' and adding definitions for terms associated with medical devices and clinical trials.
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Dec 12, 2025
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Pharmacy%20Practice%20Regulations.pdf
▶ Summary
This document is an extraordinary gazette published by the authority concerning regulations under the Indian Drugs Act, 1948. It details the rules and definitions related to drug examination and manufacturing in the context of Indian pharmaceutical regulations. The document was published by the Indian government with the intention of amending and updating drug-related regulations.
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New Drugs and Clinical Trials Rules, 2019.pdf
▶ Summary
This document is the New Drugs and Clinical Trials Rules, 2019 issued by the Central Drugs Standard Control Organization under the Ministry of Health and Family Welfare, Government of India. It outlines the regulations for new drugs, investigational drugs, clinical trials, and related studies and defines key terms and guidelines relevant to these activities. The rules are established under the Drugs and Cosmetics Act and detail procedures for conducting clinical trials and bioequivalence studies.
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document |
Gujarat FDA - News Feed
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Cosmetics Rules 2020.pdf
▶ Summary
This document contains the finalized 'Cosmetics Rules, 2020' issued by the Central Drugs Standard Control Organization under the Ministry of Health and Family Welfare, India. It outlines the regulations applicable to cosmetics, including definitions, roles of licensing authorities, and enforcement procedures. The rules are based on earlier drafts and public consultations, and they provide a comprehensive regulatory framework under the Drugs and Cosmetics Act, 1940.
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order |
Gujarat FDA - News Feed
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Dec 12, 2025
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Medical Devices Rules, 2017.pdf
▶ Summary
The document is the Medical Devices Rules, 2017 issued by the Central Drugs Standard Control Organization, Ministry of Health and Family Welfare, Government of India. It outlines the regulations for medical devices, including definitions, applications, and administrative procedures. This document serves as a legal framework for the management and administration of medical devices in India, effective from January 1, 2018.
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document |
Gujarat FDA - News Feed
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Drugs Rules, 1945.pdf
▶ Summary
This document is a comprehensive compilation of amendments to the Drugs Rules, 1945, managed by the Central Drugs Standard Control Organization under the Indian Ministry of Health and Family Welfare. It covers the regulations and procedural details for drug regulation in India, including definitions and roles of various authorities, and is amended as per the latest gazette notifications. The document ensures users are aware of the correct rules and invites them to report any discrepancies to the CDSCO.
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Gujarat FDA - News Feed
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Dec 12, 2025
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Drugs and Cosmetics Act, 1940.pdf
▶ Summary
This document is the Drugs and Cosmetics Act, 1940, issued by the Central Drugs Standard Control Organization under the Ministry of Health and Family Welfare, Government of India. It outlines the legal framework for the regulation of drugs and cosmetics, including definitions, the establishment of advisory boards, and the functioning of government analysts and inspectors. The act extends to the whole of India, and specifies its commencement and application to states like Jammu and Kashmir.
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BIS_Rules_2018.pdf
▶ Summary
This document is a gazette notification published by the Government of India, detailing regulations under the Indian Standards Bureau Act, 2016. It includes definitions and the formation of a governing council for standardization procedures. The document specifies administrative structures and member compositions for overseeing the implementation of these standards.
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order |
Gujarat FDA - News Feed
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Dec 12, 2025
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168684.pdf
▶ Summary
This document is the Bureau of Indian Standards Act, 2016, published by the Ministry of Law and Justice. It establishes the Bureau of Indian Standards as a national body for standardization, conformity assessment, and quality assurance of goods and services in India. The document details definitions, procedures, and responsibilities related to standards adherence across various sectors.
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Gujarat FDA - News Feed
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Dec 12, 2025
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248047.pdf
▶ Summary
This document is the Jan Vishwas (Amendment of Provisions) Act, 2023, enacted by the Indian Parliament to amend various enactments to decriminalize and rationalize offences, enhancing government trust and easing business operations. It details changes in fines and penalties and updates several legislative provisions affecting the press and newspaper registration. The act received presidential assent on August 11, 2023.
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Dec 12, 2025
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47of2023_250882.pdf
▶ Summary
The document is an act from the Parliament of India, known as the Bharatiya Sakshya Adhiniyam, 2023, which consolidates and provides general rules and principles of evidence for fair trials. It outlines definitions, applications, and principles related to evidence in judicial proceedings. The act received the President's assent on December 25, 2023, and details its application to legal contexts, excluding affidavits and arbitration processes.
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