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Regulatory & industry news

What changed across CDSCO, EU MDR, NABL, ISO, BIS & CPCB — and who it affects.

BreakingCDSCO extends voluntary registration window for Class A & B medical devices
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Regulatory

CDSCO extends voluntary registration window for Class A & B medical devices

The Central Drugs Standard Control Organisation has issued a fresh notice clarifying timelines for importers and manufacturers of low-risk medical devices to complete registration under the Medical Device Rules, easing the transition for IVD and Class A/B device suppliers.

CDSCOApr 22, 2026

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CPCB sharpens EPR enforcement for plastic packaging used by device importers

Mar 02, 2026

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BIS notifies new performance standards for select in-vitro diagnostic reagents

Feb 14, 2026

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CDSCO expands online SUGAM submissions to speed up import licensing

Jan 28, 2026

Industry

Domestic medical-device manufacturing push gathers pace under PLI scheme

Jan 10, 2026

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