Diagnostic Registration Consultant in Noida
Diagnostic Registration Consultant in Noida: The Complete Guide for Labs and Pathology Centers Healthcare in India is growing fast, and the demand for labs, pathology…
Diagnostic Registration Consultant in Noida: The Complete Guide for Labs and Pathology Centers Healthcare in India is growing fast, and the demand for labs, pathology…
BIS has made FMCS applications fully digital from 1 June 2026, while a new electrical appliances QCO adds 90+ product categories with an October 2026 deadline. Here’s what foreign manufacturers must do now.
CDSCO’s October 2025 draft guidance on Medical Device Software is reshaping how SaMD and AI/ML tools are classified and licensed in India. Here’s what you need to act on.
BIS adds furniture to mandatory certification, extends Scheme X deadline to September 2026, and expands CRS to 70+ electronics categories.
India’s cosmetic import rules are tightening in 2026. This practical guide covers COS-1 to COS-2 approval, fees, timelines, and post-approval compliance under the Cosmetics Rules, 2020.
India’s Battery Waste and E-Waste EPR frameworks have been significantly tightened for FY 2025–26 and beyond. Here’s what producers and importers must do now.
India’s PWM Amendment Rules 2026 (G.S.R. 237(E)) impose binding recycled content targets, new importer obligations, and ₹1 crore penalties. Act before June 30.
he Central Drugs Standard Control Organization (CDSCO) has issued a new public notice dated 4 May 2026 regarding the disposal and rejection of long-pending applications
The March 2026 FSSAI licensing overhaul changes the rules for nutraceutical FBOs — from perpetual validity to new thresholds. Here’s what you must do now.
India’s NDPS regulatory landscape shifted significantly in late 2025 and early 2026. Here’s what pharmaceutical companies must act on now.