Discover how SEQOVA supported a pharma manufacturer in achieving full system validation before production go-live. From MES and LIMS to ERP and SCADA, we delivered a structured CSV approach aligned with EU Annex 11—ensuring digital compliance from setup to sustained operations.
From Setup to Compliance: CSV That Delivers Read More »
Step-by-step guide to FDA drug registration with timelines, costs, and approval shortcuts Understanding Drug Classification Registering a medicinal product to
A Comprehensive Guide to Registering a Medicinal Product in the U.S. Read More »
Pharma M&A trends, key drivers, and top 2023–2024 deals A Structural Pillar of Pharma Strategy: Mergers and Acquisitions Mergers and
Mergers and Acquisitions in the Pharma Industry: A Strategic Imperative Read More »
Discover how market reports guide strategic decisions in pharma Market Reports: Intelligence for Decision Making In the fast-paced and highly
The Power of Market Reports in the Pharma Industry: Why They Matter Read More »
Discover the key advantages & global trends in CDMOs Introduction: CMO vs. CDMO – What’s the Difference? In the ever-evolving
The Rise of CDMOs: Transforming Pharmaceutical Outsourcing Read More »
Uncover how drug shortages occur globally, their impacts and the potential solutions. Understanding Drug Shortages Drug shortages have become an
Understanding the Scenario In a landmark transaction, two major multinational corporations (MNCs) agreed to transfer an extensive portfolio of over
Discover the nuances of registering your medicinal product in the EU. Medical Product Registration in the EU: “How is it
Basics of Registering a Medicinal Product in the EU Read More »
Case Brief Scenario Serious adverse event (SAE) reports are now generated directly from electronic data capture (EDC) systems. However, formal
Streamlining Serious Adverse Event Narratives for Clinical Study Read More »
Discover how our approach simplifies literature searches for DSUR, saving time and improving accuracy in safety reporting through streamlined processes.
Simplifying Literature Searches for DSUR Read More »
