Global Cosmetic Compliance
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Regulatory Guidelines for Sampling of Drugs, Cosmetics and Medical Devices by Drug Inspectors of Central and State Drug Authorities (May 2026 Revised Version)
Local Title:
Revised Regulatory Guidelines for Sampling of Drugs, Cosmetics and Medical Devices by Drug Inspectors of Central and State Drug Authorities
Country/Region:
India
Competent Authority:
Central Drug Standards Control Organization
Type:
Guideline
Status:
In force
Release Date:
2026-05-26
Implementation Date:
2026-05-26
Document
Language Source Title Access
EN
Official Regulatory Guidelines for Sampling of Drugs, Cosmetics and Medical Devices by Drug Inspectors of Central and State Drug Authorities (May 2026 Revised Version)
Summary

On May 26, 2026, India's CDSCO released revised Regulatory Guidelines for Sampling of Drugs, Cosmetics and Medical Devices by Drug Inspectors of Central and State Drug Authorities. The update strengthens post-market surveillance and regulatory enforcement by expanding reporting requirements for products identified as Not of Standard Quality (NSQ) or spurious.

The revised document supersedes the February 2024 version and largely keeps the existing structure, covering sampling plans, sample selection, sampling locations, sample quantities, timelines, database monitoring, NSQ and spurious alerts, and testing laboratories.

History
2026-05-26
Regulatory Guidelines for Sampling of Drugs, Cosmetics and Medical Devices by Drug Inspectors of Central and State Drug Authorities (May 2026 Revised Version)
In force
Release Date: 2026-05-26
Implementation Date : 2026-05-26
2024-02-09
Invalid
Release Date: 2024-02-09
Implementation Date : 2024-02-09
Noteworthy Information
User Guide