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199 documents matching
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IN FORCE
130 PRO Details of Zonal, Sub zonal offices of CDSCO 2024-Jan-09 26 KB
IN FORCE Import policy & restrictions ·?
109 NOC's for manufacture of Unapproved/Banned/New Drugs Solely for Export Purpose 2024-Apr-30 454 KB
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100 Names of countries under the Rule 101 of New Drugs and Clinical Trial Rules 2019 related to new drug approval 2024-Aug-07 280 KB
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183 Classification of Medical Device Pertaining to Obstetrical and Gynecological Under the provision of Medical Devices Rules 2017 2022-Jun-03 529 KB
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167 Classification of Medical Device pertaining to Oncology under the provisions of Medical Devices Rules, 2017 2022-Oct-11 817 KB
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99 Appointment of CPIO for the purpose of RTI Technical Matters 7 Aug 24 2024-Aug-07 96 KB
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165 Inspection/Audits of Pharmacovigilane(PV) system of importers and manufactures of human vaccine 2022-Dec-28 322 KB
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177 Notice dated July 11 2022 2022-Jul-11 370 KB
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143 Notice regaring submission of documents in scan copy 2023-Oct-12 568 KB
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116 Notice to All stakeholders for Strengthening of Private Medical Device Testing Laboratory 2024-Apr-03 388 KB
Strengthening of private Medical Devices Testing Laboratory in the country
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127 Launching of additional Forms on National Single Window System NSWS Portal 2024-Jan-16 7274 KB
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41 Notice for inviting comment to ensure a level playing field in new drug approval in India 2025-Oct-08 597 KB
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111 Manufacturing and marketing of unapproved drug Meropenam 1gm + EDTA for Injection 2024-Apr-16 366 KB
IN FORCE Procedural & compliance ·?
189 Classification of Medical Device pertaining to General Hospital under the provisions of Medical Devices Rules 2017 2022-Mar-16 813 KB
IN FORCE Import policy & restrictions ·?
4 Rejection and Debarment of application for submission of fabricated documents by firm M/s. DMF Cosmo Private Limited 2026-May-15 397 KB
DMF Cosmo Pvt. Ltd.
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201 Module for online processing of applications for registration of BA BE study centres (CT-08) 2021-Oct-01 303 KB
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85 Prohibits to manufacture, sale and distribution and use of drug Nimesulide and its formulation for animal use with immediate effect 2025-Feb-20 287 KB
IN FORCE Export policy & incentives ·?
124 Online application for Neutral Code for manufacturing of Medical Devices for export purpose 2024-Feb-12 305 KB
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128 Month wise Tentative Schedule of SEC (Vaccine) meetings of the Year 2024 2024-Jan-12 18 KB
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164 Month wise Tentative Schedule of SEC (Vaccine) meetings of the Year 2023 2023-Jan-20 18 KB
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191 Month wise Tentative Schedule of SEC (Vaccine) meetings of the Year 2022 2022-Feb-17 10 KB
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33 MedTech Mitra's In-Vitro Diagnostic Innovators Handbook 2025-Dec-05 5974 KB
HS 01HS 02HS 03HS 04
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95 MEDICAL DEVICE ADVERSE EVENT REPORTING FORM Version 1.2 2024-Oct-08 656 KB
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92 Merged existing Medical Devices risk-classification 2025-Jan-01 33581 KB
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145 List of medical devices testing laboratory (MDTL) for carry out test or evaluation of medical device on behalf of manufacturer registered with CDSCO under MDR 2017 2023-Sep-15 1635 KB
Bharat Test TL/MD/2022/00001 1 1. Ultrasonic Physiotherapy . House Private Equipments Class B Ltd.Manisha TL/MD/2022/000012 1. Sterile Blood Bags Class A Analytical 2. Sterile Catheters Class B Laboratories Pvt. 3. Disposable Hypodermic Needles Ltd.BEE PHARMO<br>LABS Pvt. Ltd.
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197 List of approved veterinary vaccines 2021-Dec-02 1138 KB
Virbac Animal Health India Pvt. Ltd.Abic Biological Laboratories Ltd.Boehringer Ingelheim India Pvt. Ltd.
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187 List of laboratories for conducting Performance evaluation of IVD analyzers, instruments and software 2022-May-05 103 KB
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157 List of Notified Bodies registered with CDSCO under MDR, 2017 2023-Apr-03 830 KB
Intertek India Pvt. Ltd.TUV Rheinland India Pvt. Ltd.TUV Sud South Asia Pvt. Ltd.
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175 List of the Certified Medical Device Testing Laboratory under MDR, 2017 2022-Aug-17 5938 KB
StarImaging&<br>Path Lab Pvt. Ltd.SreeChitra<br>Tirunal Institute For<br>Medical Sciences&<br>Technology
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58 Issues related to safety of Ranitidine drug due to presence of NDMA impurity 2025-Jul-24 71 KB
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42 Strict compliance with the Drugs Rules 1945 for testing of raw materials and finished formulations 2025-Oct-07 418 KB
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63 Regulatory requirements for outsourcing sterilization activity of medical devices by a manufacturer under Medical Device Rules 2017 2025-Jun-24 713 KB
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38 Digital Monitoring System on the ONDLS portal for monitoring the supply chain of high-risk solvents 2025-Oct-22 577 KB
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147 Receipt of Cough Syrup of same batch No.by two different NABL Accredited Government Laboratories Manufactured by the same Manufacturers/Exporters 2023-Jul-28 394 KB
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198 Public notice on draft Recruitment rules for the post of LDC Central Drugs Laboratory Kolkata 2021-Nov-26 412 KB
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50 Inviting comments on consideration of the proposal regarding problem faced by the blind or visually impaired people to read medicines tablets/capsules strips 2025-Sep-09 714 KB
Inviting comments on consideration of the proposal regarding problem faced by the blind or visually impaired people to read medicines tablets/capsules strips
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52 Inviting comments on standard IVD evaluation protocols drafted by ICMR and CDSCO 2025-Aug-26 5218 KB
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54 Inviting comments on standard IVD evaluation protocol drafted by ICMR and CDSCO 3 2025-Aug-12 4130 KB
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34 Risk classification list of medical devices pertaining to Interventional Radiology 2025-Nov-27 441 KB
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96 Draft Guidelines on Good Clinical Practices 2024-Sep-12 3315 KB
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158 Implementation of Pre-shipment inspection under testing 2023-Jun-20 4419 KB
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140 Updation of classification in IVD medical devices under the provision of MD Rules 2017 2023-Oct-25 1473 KB
IN FORCE Export policy & incentives ·?
149 Daily Updation of No.of Batches of Cough syrup sample for Export at Different Laboratories for testing Request not to submit any sample of cough syrup to IPC Ghaziabad and CDTL Mumbai Lab 2023-Ju
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44 ICMR-CDSCO Standard Performance Evaluation Protocols 2025-Sep-17 7383 KB
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11 Manufacturing and marketing of unapproved drug product Sodium Hyaluronate Eye Drops 0.3% w/v 2026-Mar-18 351 KB
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134 CDSCO updated list of laboratories to conduct Performance evaluation of IVDs dated 29.11.23 2023-Dec-06 654 KB
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153 CDSCO updated list of Laboratories for conducting Performance Evaluation of In - Vitro Diagnostic Medical Device 2023-May-22 214 KB
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12 Guidance document on dossier based licensing of Drugs for uniform product licensing in the country 2026-Mar-17 822 KB
IN FORCE Procedural & compliance ·?
67 Guidance document on disposal of expired/ unused drugs 2025-May-27 588 KB
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89 Guidance document Validation of Rapid Diagnostics for Pathogen Identification and Antimicrobial Susceptibility Testing (AST) 2025-Jan-16 2642 KB
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