Oct 14, 2026

CDSCO Issues Draft Guidance for Manufacturing In-Vitro Diagnostic Medical Devices in India

CDSCO Draft IVD Manufacturing Guidance 2026 | ACPL ACPLACCREDITED CONSULTANTS PVT. LTD.Visit ACPL Website Medical Device Regulatory Update · 9…

Oct 14, 2026

CDSCO Clarifies Export NOC Requirements for Already Approved r-DNA Drug Products

CDSCO Export NOC for r-DNA Drugs: 2026 Update | ACPL ACPL ACCREDITED CONSULTANTS PVT. LTD. Visit ACPL Website Pharmaceutical Regulatory…

Sep 16, 2026

Make in India and Public Procurement of Medical Devices: What Manufacturers Should Know

Medical Devices CDSCO Consultant in India

Aug 31, 2026

Medical Devices (Third Amendment) Rules, 2026: EU Countries Added to Rule 63 | CDSCO Update

CDSCO Medical Device Regulatory Update Medical Devices (Third Amendment) Rules, 2026: EU Countries Added to Rule 63 Understanding the key…

Aug 26, 2026

PESO License in India: Complete Guide to Requirements, Process, Documents and Fees

Learn about PESO License in India, applicable rules, eligibility, documents, application process, fees, renewal and compliance. Get PESO consultancy support…

Aug 17, 2026

Entering the Indian Pharmaceutical Market: A Practical Guide for European Pharma Companies

Entering the Indian Pharmaceutical Market: A Practical Guide for European Pharma Companies India’s pharmaceutical market is massive, but it’s not…

Aug 14, 2026

CPCB’s New “Lost Credentials” Facility: A Simple Guide for EPR Portal Users

CPCB just made life easier for anyone managing EPR accounts with their new “Lost Credentials” feature. If you’re stuck because…

Aug 12, 2026

CDSCO Clarifies Regulatory Pathway for Globally Unapproved New Drugs After Phase III Global Clinical Trials

CDSCO clarification 10 August 2026, globally unapproved new drugs India, Form CT-18, NDCT Rules 2019, Phase III Global Clinical Trial…

Aug 10, 2026

BIS Certification: Important Reasons Why Your BIS Application Gets Rejected

BIS Certification, BIS Registration, BIS Application Rejection, BIS Certification Consultant, BIS Registration Consultant, BIS CRS Registration, ISI Mark Certification, BIS…

Aug 6, 2026

CDSCO Guidance on Common Submission Format for Drug Imports in India: What Pharma Companies Really Need to Know

India’s Central Drugs Standard Control Organization (CDSCO) just rolled out a new Guidance Document for importing and registering drugs—both bulk…