Pharma Manufacturing
Inside PMITS Ahmedabad, 7 July 2026. 130 delegates, India's top pharma manufacturing IT leaders, on MES, CSA, GAMP 5, and the paperless transition.
Mrudula Kulkarni | Jun 23, 2026
GAMP 5 Second Edition for MES: A Practical Validation Guide
Mrudula Kulkarni | Jun 22, 2026
7 Challenges in scaling RNA Therapeutics Manufacturing
Mrudula Kulkarni | Jun 18, 2026
What Are The Regulatory Challenges In Nanotechnology-Based Therapeutics?
Simantini Singh Deo | Jun 16, 2026
Other trending pieces on pharma manufacturing you may like to read
Inside the Pharma Manufacturing IT Summit, Ahmedabad: Why the Factory Floor Finally Gets a Seat at the Table
Inside PMITS Ahmedabad, 7 July 2026. 130 delegates, India's top pharma manufacturing IT leaders, on MES, CSA, GAMP 5, and the paperless transition.
by Mrudula Kulkarni
GAMP 5 Second Edition for MES: A Practical Validation Guide
GAMP 5 Ed.2 recalibrates MES validation around risk, not paperwork. Here's the practical classification framework pharma teams need.
by Mrudula Kulkarni
7 Challenges in scaling RNA Therapeutics Manufacturing
mRNA vaccines proved the science works. Scaling RNA therapeutics manufacturing is the real challenge, 7 bottlenecks the industry faces.
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What Are The Regulatory Challenges In Nanotechnology-Based Therapeutics?
1,200+ nanomedicine trials are active globally, yet only 50-80 have reached approval. The regulatory gaps pharma must solve.
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The Hidden Tax on Pharma: Mastering the Cost of Quality Before It Masters You
Cost of Quality in pharma explained — PAF model, COPQ benchmarks, real biotech case study, key metrics and how eQMS reduces quality failure costs.
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