| 1 |
Restriction on shifting/reallocation of IT equipment without prior intimation and approval of Administration and IT cell of CDSCO(HQ) |
2026-May-13 |
|
90 KB |
| 2 |
Submission of Periodic Safety Update Reports (PSURs) for New Drugs via SUGAM Portal on deferred basis in case of delayed Marketing after Approval |
2026-Apr-21 |
|
341 KB |
| 3 |
Circular on Implementation of Prior intimation System for Form CT-05 application (for export purpose only) w.e.f 21.04.2026 in pursuance of G.S.R 50(E) dated 21.01.2026 |
2026-Apr-20 |
|
4025 KB |
| 4 |
Streamlining the procedure for disposal of applications for "Written Confirmation" (WC) for Active Substances Exported to the EU for Human Use in accordance with Article 46(2)(b) of Directive 2001/83/EC received in CDSCO SUGAM Portal |
2026-Mar-27 |
|
29536 KB |
| 5 |
Import, manufacturing, sale etc. of medical devices intended for InVitro Fertilization viz., IUI (Intrauterine Insemination) kits, centrifuge for sperm washing etc. used for Assisted Reproductive Technology related procedures |
2026-Mar-27 |
|
454 KB |
| 6 |
Online Applications for grant of license in Form 28-D/28-DA for r-DNA products |
2026-Mar-10 |
|
435 KB |
| 7 |
Online Applications for Post Approval Changes (PAC) w.r.t Marketing Authorization (MA) for r-DNA products |
2026-Mar-09 |
|
397 KB |
| 8 |
Implementation of Prior intimation System for Forms CT-10, CT-12 and CT-13 in pursuance of G.S.R. 46(E) dated 20.01.2026 |
2026-Mar-06 |
|
57 KB |
| 9 |
Testing of drugs for grant of permissions for import/manufacture of New Drug for sale or for distribution and Issuance of RC for import of Drugs etc |
2026-Feb-24 |
|
92 KB |
| 10 |
New provision for Risk Classification of Medical Devices on the CDSCO Online System for Medical Devices |
2025-Dec-05 |
|
251 KB |
