By Darshan Singh, 23 years in pharmaceutical QC, QA and regulatory affairs · Reviewed against the source texts on 29 September 2026 Short answer Validation is documented evidence that premises, utilities, equipment, processes, cleaning procedures, test methods and computerised systems…
Data verified as of June 19, 2026, sourced from the NSE Nifty Pharma Index free-float market capitalisation weightage. Rankings shift as share prices move — this page is maintained and re-checked against live exchange data, not a one-time snapshot. Twenty-three…
Purchasing a pharmaceutical company is a significant investment decision that requires a thorough valuation to ensure a successful and profitable decision. In this blog post, we will explore the importance of valuation, key factors to consider, the role of experts,…
For pharmaceutical manufacturers in India, complying with Schedule M – the cornerstone of Good Manufacturing Practices (GMP) – has long been the game. But the winds of change have blown, ushering in a revised Schedule M, promising a more robust…
Quality assurance and Quality control both terms seem very similar in general but are very different in view of the roles they play in a company. In pharmaceutical manufacturing companies, both QA and QC have predefined roles and functions. These…
Published 12 February 2023 · Fully revised 20 September 2026 · Darshan Singh, 23 years in pharmaceutical QA, QC and drug regulatory affairs Short answer Kala Amb, in Sirmaur district of Himachal Pradesh, is one of 118 pharmaceutical clusters formally…