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Pharma Manufacturing

How To Write a CAPA Report That Stands Up To Any Audit

A practical guide to writing CAPA reports that meet GMP, FDA, and ISO standards with strong root cause analysis.

Mrudula Kulkarni | Apr 10, 2026

Knowledge Hub

Computer System Validator (CSV) vs. Computer System Assurance (CSA): What Are the Main Differences?

Guide to Computer System Validation (CSV) vs Computer Software Assurance (CSA) in pharma with key differences and risk-based approach.

Vaibhavi M. | Apr 10, 2026

Microbiology Insights

Gaps in Antimicrobial Stewardship Programmes in Asia: A Survey of 10 Countries

Why Asia's antimicrobial stewardship programmes are falling short — a 10-country survey of 6 gaps blocking real AMR progress

Mrudula Kulkarni | Apr 02, 2026

Pharma Manufacturing

5 End-to-End Manufacturing Traceability Software Transforming Pharma Supply Chains

5 pharma traceability software tools that close supply chain gaps, speed up recalls, and turn compliance into control.

Mrudula Kulkarni | Mar 27, 2026

Microbiology Insights

Bridging the Translational Research Gap: A Successful Partnership Involving a Physician and a Scientist

How physician-scientist partnerships bridge the translational gap in microbiology and drive real-world solutions for India's AMR crisis.

Nandini Swaminathan, PhD | Mar 24, 2026

AI in Pharma

7 Reasons Why AI Strategy Fails In Pharma — And How To Fix It

7 reasons AI strategy fails in pharma — from data gaps to regulatory misalignment — and how to fix each one.

Vaibhavi M. | Mar 20, 2026

Pharma Manufacturing

Real-Time Release Testing (RTRT): Replacing Traditional QC Models In Pharma

How Real-Time Release Testing is replacing traditional QC with faster, smarter, data-driven pharmaceutical manufacturing.

Simantini Singh Deo | Mar 18, 2026