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Insights & Blog

Regulatory updates, compliance insights, and industry analysis from the ACPL team.

Regulatory Updates
Aug 3, 2026

FSSAI Packaged Drinking Water Rules 2026: BIS Mark Scrapped

FSSAI has scrapped mandatory BIS certification for packaged drinking water and replaced it with a strict new testing regime from…

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Aug 1, 2026

Import of Medical Devices into India: CDSCO Import Licence Process

Import of Medical Devices into India: CDSCO Import Licence Process

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Aug 1, 2026

Bringing Medical Devices into India: Your Practical Guide to CDSCO Rules

earn the complete CDSCO medical device import process in India, including eligibility, documentation, licensing, compliance, and regulatory requirements under the…

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Aug 1, 2026

DSIR Recognition and Approval Services in India: A Practical Guide for R&D Organizations

Learn about DSIR recognition, Section 35(2AB) historical approvals, R&D centre registration, renewals, and compliance services. ACPL provides complete DSIR consultancy…

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Jul 30, 2026

PESO (Petroleum and Explosives Safety Organisation) Registration & Licensing Services in India

PESO, or the Petroleum and Explosives Safety Organisation, stands as India’s central authority for keeping hazardous substances in check. They’re…

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Regulatory Updates
Jul 27, 2026

Plastic EPR Enforcement 2026: Audits, Customs Blocks & Penalties

CPCB has moved from rule-making to enforcement on plastic EPR—Registered Environment Auditors, customs blocks, and crore-level penalties are now live.…

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ACPL
Jul 25, 2026

Navigating the Latest CDSCO Circular: What It Means for India’s Cosmetics Sector

Regulatory compliance has always been the backbone of a trustworthy supply chain, but a recent directive from the Central Drugs…

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Jul 23, 2026

CDSCO Prohibits 16 Fixed Dose Combinations (FDCs): Key Regulatory Update for the Pharmaceutical Industry

CDSCO Bans 16 Fixed Dose Combinations: What Pharma Companies Need to Know Effective June 11, 2026, the Central Drugs Standard…

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Jul 23, 2026

CDSCO Issues Final Guidance on Medical Device Software under MDR 2017: What Manufacturers Need to Know

CDSCO Issues Final Guidance on Medical Device Software under MDR 2017: What Manufacturers Need to Know

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Regulatory Updates
Jul 20, 2026

Footwear QCO 2026: DPIIT Extends Stock Deadline to 2027

DPIIT's June 2026 footwear QCO amendments extend the legacy stock sell-off deadline to July 31, 2027 and ease R&D import…

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