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From approvals and documentation to lifecycle compliance and market-entry strategy, Aloft Insights helps businesses understand evolving regulatory expectations and make confident decisions.
CDSCO has issued a public notice regarding the disposal/rejection of long-pending applications on the SUGAM portal where queries raised by the authority are still awaiting response from applicants.
Implementation of Prior Intimation System for Form CT-05 applications (for export purposes only) in pursuance of G.S.R. 50(E) is live on the SUGAM Portal as of 21 April 2026.
CDSCO regularly publishes updates on NSQ drugs — samples tested by government laboratories and found not meeting prescribed quality standards under the applicable regulatory framework.
Medical devices in India are classified into 4 risk-based classes (A to D) under the Medical Device Rules, 2017 — determining licensing authority and approval pathway.
Comprehensive overview of medical device licenses under the Medical Device Rules, 2017 — covering manufacturing (Class A/B/C/D), loan licenses, import, test licenses, clinical investigations, and IVDs.
India's cosmetic regulatory framework requires importers and foreign cosmetic brands to obtain appropriate registration before importing cosmetic products. Understand the difference between Form COS-1 (application) and Form COS-2 (registration certificate) under the Cosmetics Rules, 2020.
A visual guide to mandatory cosmetic labelling elements required for import and sale in India under the Cosmetics Rules, 2020.
India follows the Nice Classification system — 45 classes total (Classes 1-34 for goods, 35-45 for services). Choosing the right class is essential for valid, enforceable trademark protection.
Our experts can help you interpret CDSCO circulars, plan compliance responses, and stay ahead of evolving regulatory expectations.
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