Regulatory updates, compliance insights, and industry analysis from the ACPL team.
CDSCO Releases Final Guidance on Medical Device Software under MDR 2017: What You Need to Know Published: July 2026 On…
Read MoreDPIIT's June 2026 footwear QCO amendments extend the legacy stock sell-off deadline to July 31, 2027 and ease R&D import…
Read MoreFSSAI's March 2026 licensing overhaul and milk-sector advisory bring perpetual licences, new turnover slabs, and high-risk inspections for dairy. Here's…
Read MoreIndia's June 2026 narcotics enforcement surge and the DCC-approved real-time tracking portal raise the bar for pharmaceutical supply chain compliance.
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Materiovigilance Services in India: Safeguarding Medical Device Safety and Performance India’s medical device industry is expanding fast, but that growth…
Read MoreA new controlled substance under NDPS was notified in March 2026 with stock and registration deadlines in July–August 2026. Here's…
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India Market Entry Strategy for Medical Device Companies: A Complete Regulatory Guide by ACPL India’s medical device market is booming,…
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Looking for a Regulatory Affairs Consultant in Noida? You’re in the right place. The world of pharmaceuticals, medical devices, food,…
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India’s pharmaceutical market is huge—and growing by the day. For global pharmaceutical companies, biotechs, and healthcare innovators, it offers a…
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