All Extracted Documents - Website Tracker

Title	Type	Source	Release Date	Scraped	Download	Status
CLAA Medical Device Approvals January-July 2017 CLAA_Year_2017.pdf ▶ Summary This document provides a detailed statement regarding the grant of approvals by the Central Licensing Authority (CLAA) for the manufacture of various notified medical devices from January 2017 to July 2017. It includes information about specific medical products, their manufacturers, and the validity of their licenses. The data lists manufacturers from various locations along with the materials used and the types of medical devices approved.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✓ Relevant
CLAA Approved Medical Device Manufacturers 2016 CLAA_Year_-2016.pdf ▶ Summary This document provides a list of manufacturers and products approved by the CLAA for the manufacture of various medical devices, specifically intravenous cannulas, from January 2016 to December 2016. It includes details such as manufacturer names, product descriptions, manufacturing license numbers, and validity dates. The primary purpose of the document is to indicate the status of product approvals within the specified timeframe.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✓ Relevant
2015 Medical Device Manufacturing Approvals Notice CLAA_Year_2015.pdf ▶ Summary This document is a public notice from the Central Licencing Authority (CLAA) detailing the approvals granted for the manufacture of notified medical devices from January to December 2015. It lists various manufacturers along with the specific medical devices they are authorized to produce, along with licensing information. The notice is intended for regulatory compliance and public awareness regarding approved medical device manufacturing.	public notice	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✓ Relevant
Manufacturing Licenses for Medical Devices in 2014 CLAA_Year_2014.pdf ▶ Summary This document lists the manufacturing licenses granted for notified medical devices in India during 2014. It details the manufacturers, products, and the validity periods of the licenses. The focus is on providing a comprehensive overview of approved manufacturers and their product offerings in the medical device sector.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✗ Filtered
CLAA Medical Device Approvals Overview 2013 CLAA_Year_2013.pdf ▶ Summary This document lists the status of approvals granted by the CLAA for the manufacture of various notified medical devices from January 2013 onwards. It includes detailed information about multiple manufacturers, the products they are licensed to produce, and the validity of these manufacturing licenses. Each entry includes the manufacturer's location, the specific medical devices approved, and the serial numbers and validity dates of the manufacturing licenses.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✗ Filtered
CDSCO Medical Device Approvals 2012 Public Notice CLAA_Year_2012.pdf ▶ Summary The document is a statement from the CDSCO detailing the status of manufacturing approvals for various medical devices issued by the CLAA from January to December 2012. It lists manufacturers, their products, and the respective licenses and validity periods. This serves as a public record of approved medical devices manufactured during that period.	public notice	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✓ Relevant
Medical Device Approval Licenses January-August 2011 CLAA_Year_2011.pdf ▶ Summary This document contains a list detailing the grant of approval for the manufacture of various medical devices by several manufacturers, with each entry including the manufacturer's name, product groups, and license numbers along with their validity periods. The content primarily lists licenses for different medical devices approved from January 2011 to August 2011. The document seems to target regulatory audiences interested in the licensing and approval status of medical manufacturing companies.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✗ Filtered
2010 CLAA Manufacturer Approvals for Medical Devices CLAA_Year_2010.pdf ▶ Summary This document appears to be a record listing manufacturers granting approvals by CLAA for the production of various medical devices between January and December 2010. It includes details such as the names of manufacturers, types of medical devices, and manufacturing license numbers along with their validity periods. The document does not seem recent or directly matching typical public notice formats but pertains generally to regulatory procedures in the medical device manufacturing sector.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✗ Filtered
Medical Device Approval Process Flowchart Approval_process_flowchart_MD_hardcopy2.pdf ▶ Summary The document outlines the approval process for applications received in hard copy related to medical devices. It details the steps from submission and document review to eventual approval or query if there are deficiencies. The information appears to be procedural guidance intended for applicants seeking approval for medical devices.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✗ Filtered
Medical Device Approval Process Flowchart Approval_process_flowchart_MD_Online1.pdf ▶ Summary This document outlines the approval process for applications related to medical devices submitted via the Online Sugam Portal. It details the steps followed in the review process including receipt by a nodal officer, forwarding to reviewing officers, and addressing any deficiencies in submitted documents. The document serves as a guide for applicants on how their applications are processed.	document	CDSCO - Public Notices Unknown	—	Dec 15, 2025	pdf ↓	✗ Filtered
CDSCO Public Notice on Drug Approval Feedback Public Notice 10 ▶ Summary The Central Drugs Standard Control Organization (CDSCO) has issued a public notice inviting comments on ensuring a level playing field in the approval process for new drugs in India. The notice highlights discrepancies between first-time and subsequent applicants in terms of costs and compliance requirements for drug approvals. Stakeholders are encouraged to provide feedback and suggestions to help formulate a balanced policy.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant
Guidance on Medical Device Software Regulations Public Notice 9 ▶ Summary This document, issued by the Medical Devices Division of the Central Drugs Standard Control Organization (CDSCO), is a guidance document on Medical Device Software. It aims to create public awareness about regulations related to medical device software and invites stakeholder comments on the draft. The document provides an index of topics covered, such as classification, regulatory pathways, and licensing related to medical device software.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant
BIS Standards for Surgical Instruments and Specifications Public Notice 8 ▶ Summary The document is a comprehensive list of BIS standards for various medical equipment and hospital planning, specifically focusing on surgical instruments. It categorically lists numerous instruments with their IS specifications, denoting patterns, shapes, and dimensions. Issued by the Medical Equipment and Hospital Planning Department, it serves as a reference for standardized medical devices.	document	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✗ Filtered
CDSCO Public Notice on Digital Monitoring System for Solvents Public Notice 7 ▶ Summary This document is a public notice issued by the Central Drugs Standard Control Organisation (CDSCO), India, regarding the implementation of a Digital Monitoring System on the ONDLS portal for monitoring the supply chain and quality of high-risk solvents. The notice instructs State/ UT Drug Controllers to ensure manufacturers obtain and register licences via the upgraded portal, outlining compliance requirements for market release of pharmaceutical solvents. It highlights the necessity of monitoring to prevent contamination incidents like the recent DEG contamination in cough syrups.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant
Post Approval Changes Submission Process for Clinical Trials Public Notice 6 ▶ Summary This public notice issued by the Central Drugs Standard Control Organization (CDSCO) informs stakeholders about the procedure for filing Post Approval Changes for Clinical Trials of Cell and Gene Therapeutic Products through the SUGAM Online portal. It emphasizes that offline submissions will not be accepted after October 24, 2025, and provides resources like user manuals and video tutorials to aid in the online filing process.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant
Classification and Exemptions for Class A Medical Devices Public Notice 5 ▶ Summary This document from CDSCO provides a list of Class A non-sterile and non-measuring medical devices that are exempt from certain provisions of the Medical Devices Rules, 2017. Manufacturers or importers must register these devices under specific chapters of the rules. The document categorizes various devices along with their intended use and classification.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant
CDSCO Public Notice on Medical Device Classification Public Notice 4 ▶ Summary This document is a public notice from the CDSCO regarding the classification of medical devices related to interventional radiology. It lists various devices, their intended use, and their risk classification. The notice serves to inform manufacturers and health professionals of the regulatory classification for these medical devices.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant
Public Notice: Radiotherapy Medical Device Classifications Public Notice 3 ▶ Summary This document is a public notice issued by a medical office concerning the classification of various medical devices used in radiotherapy. It lists multiple devices, their intended use, and associated risk classifications ranging from Class C to Class D. The notice primarily informs stakeholders about the regulatory categorization of these devices.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant
In-Vitro Diagnostic Innovators Handbook by MedTech Mitra Public Notice 2 ▶ Summary This is an In-Vitro Diagnostic Innovators Handbook published by MedTech Mitra, serving as a guiding document potentially for entities involved in the diagnostic sector. The document appears to be a comprehensive guide but lacks explicit details in the sampled pages to categorize it as an advisory, order, or public notice.	document	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✗ Filtered
Cancellation of Ethics Committee Registrations Notice Public Notice 1 ▶ Summary This document lists the suspension or cancellation of registration certificates for various ethics committees by the Central Licensing Authority (CLA). It provides the names, addresses, and registration certificate numbers of the affected ethics committees, along with the dates of cancellation. This appears to be an official notice concerning compliance and regulatory actions against specified committees.	public notice	CDSCO - Public Notices Unknown	—	Dec 12, 2025	pdf ↓	✓ Relevant

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