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407 documents matching
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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
IN FORCE
33 MedTech Mitra's In-Vitro Diagnostic Innovators Handbook 2025-Dec-05 5974 KB
HS 01HS 02HS 03HS 04
IN FORCE
95 MEDICAL DEVICE ADVERSE EVENT REPORTING FORM Version 1.2 2024-Oct-08 656 KB
IN FORCE
92 Merged existing Medical Devices risk-classification 2025-Jan-01 33581 KB
IN FORCE
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.
IN FORCE
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.
IN FORCE
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
IN FORCE
42 Strict compliance with the Drugs Rules 1945 for testing of raw materials and finished formulations 2025-Oct-07 418 KB
IN FORCE
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
IN FORCE
198 Public notice on draft Recruitment rules for the post of LDC Central Drugs Laboratory Kolkata 2021-Nov-26 412 KB
IN FORCE
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
IN FORCE
52 Inviting comments on standard IVD evaluation protocols drafted by ICMR and CDSCO 2025-Aug-26 5218 KB
IN FORCE
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
IN FORCE
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
IN FORCE
89 Guidance document Validation of Rapid Diagnostics for Pathogen Identification and Antimicrobial Susceptibility Testing (AST) 2025-Jan-16 2642 KB
HS 01HS 02HS 03HS 05
IN FORCE Export policy & incentives ·?
61 Revised Export NOC Guidance document for Manufacture of Unapproved / Approved New Drugs along with Annexures 2025-Jul-17 714 KB
IN FORCE Procedural & compliance ·?
28 Guidelines on Compounding of Offences under the Drugs and Cosmetics Act, 1940 as per Drugs and Cosmetics (Compounding of Offences) Rules, 2025 2026-Jan-01 765 KB
IN FORCE Import policy & restrictions ·?
6 Cancellation of a product 'Elementre - MD Peel-Tri AHA' under Registration Certificate No. RC/COS-005139 dated 15-Jul2O24 valid upto 14-Jul2O29 for import under Cosmetics Rules, 2020- Regarding 2026
Glow Global LLP
IN FORCE Procedural & compliance ·?
148 FAQS ON IMPLEMENTATION OF GSR 823(E) DATED 17TH NOVEMBER, 2022 WITH RESPECT TO BAR CODE OR QR CODE ON TOP 300 BRANDS 2023-Jul-25 28 KB
IN FORCE
133 To update package insertPromotional Literature of FDC of Chlorpheniramine Maleate IP 2mg Phenylephrine HCl IP 5mg drop ml- 2023-Dec-18 372 KB
IN FORCE
83 Evaluation of certain pre 1988 permitted Fixed Dose Combinations (FDCs) de novo for manufacture for sale in the country without due approval from Central Licensing Authority 24 Feb 2025 2025-Feb-24
IN FORCE Procedural & compliance ·?
27 FAQs on Drugs and Cosmetics (Compounding of Offences) Rules, 2025 2026-Jan-01 368 KB
IN FORCE
139 Notice inviting Expression of Interest for development of Digital Drugs Regulatory System 2023-Nov-02 998 KB
IN FORCE
184 Notice of Advisory for registration of blood centres on E-rakhtkosh 2022-Jun-03 5660 KB
IN FORCE
178 Notice regarding Draft of New Drugs Medical Devices and Cosmetics Bill, 2022 2022-Jul-08 1051 KB
HS 10
IN FORCE
40 Draft guidance document on conduct of Medical Device Software under MDR 2017 2025-Oct-21 1945 KB
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88 Inviting comments on standard IVD evaluation protocol drafted by ICMR and CDSCO 2 2025-Jan-29 1704 KB
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70 Inviting comments on Revised Guidelines on Similar Biologics- Regulatory requirements for Marketing Authorization in India, 2025 drafted by CDSCO 2025-May-06 1002 KB
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121 Draft CDSCO Guidance for Industry: Post Approval Changes in Biological Products 2024-Feb-28 2317 KB
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