Algeria Pharma Serialization: What’s coming in 2027 and how Vimachem can help you Algeria Pharma Serialization: What’s coming in 2027 and how Vimachem can help you Saud Kahn Senior IT Serialization Consultant Linkedin Algeria is progressing towards pharmaceutical serialization and aggregation as national requirements. As shared by market commentators, Algeria’s National Agency for Pharmaceutical Products […]
// Configurable Not Custom Why Pharma Manufacturing Needs a No-Code MES Purpose-Built for Pharma // Configurable Not Custom Why Pharma Manufacturing Needs a No-Code MES Purpose-Built for Pharma Emma Hanley Senior Product Marketing Manager Linkedin Pharmaceutical manufacturing is under increasing pressure to digitalize faster, smarter, and without compromising compliance. Regulatory scrutiny is intensifying. Global supply […]
Digital-By-Design Pharma: Why the Next Era of Pharma Manufacturing Requires MES as Core CAPEX – not a Side Project Digital-By-Design Pharma: Why the Next Era of Pharma Manufacturing Requires MES as Core CAPEX – not a Side Project Emma Hanley Pharma Digital Transformation Consultant Linkedin Reflections from the ISPE Ireland Annual Conference 2025 -“Pioneering Tomorrow: […]
Digitizing Review and Release: Smarter Workflows, Faster Reviews, Stronger Compliance with Vimachem eBR Digitizing Review and Release: Smarter Workflows, Faster Reviews, Stronger Compliance with Vimachem eBR Emma Hanley Senior Product Marketing Manager In pharma manufacturing, batch review and release can be a bottleneck. Paper-based processes slow production, introduce human error, and delay delivery, while regulators […]
Why GMP-Critical Processes Don’t Belong in ERP: W&D, Logbooks, and Electronic Batch Records (eBR) Why GMP-Critical Processes Don’t Belong in ERP: W&D, Logbooks, and Electronic Batch Records (eBR) Emma Hanley Senior Product Marketing Manager Introduction ERP systems are powerful. They centralize planning, optimize resources, and give organizations visibility across the enterprise. It’s no surprise many […]
ERP Can’t Weigh Your Batches: The Case for MES-Native Weigh & Dispense ERP Can’t Weigh Your Batches: The Case for MES-Native Weigh & Dispense Emma Hanley Senior Product Marketing Manager Introduction In pharmaceutical manufacturing, precision is everything. Every gram matter, every action must be traceable, and every record must withstand regulatory scrutiny. Yet many companies […]
Should you integrate Electronic Logbooks and OEE? Should you integrate Electronic Logbooks and OEE? Łukasz Iskra Business Development Director Linkedin As someone who regularly supports pharma and biopharma companies – especially CDMOs, CPOs – on their digital transformation journey, I often get the same question:“Should we integrate Electronic Logbooks with OEE data?”My answer is: absolutely […]
Unlocking Pharmaceutical Excellence: The FDA Quality Maturity Model Unlocking Pharmaceutical Excellence: The FDA Quality Maturity Model Nefeli Stylla QA & CSV Specialist Linkedin Are manual processes slowing down your compliance efforts? Is it time for the pharmaceutical industry to enhance operations and shift towards digital transformation? FDA’s Quality Maturity Model (QMM) can serve as your […]
// AI in Pharma MES AI In Pharma Manufacturing Execution Systems // AΙ in Pharma MES AI In Pharma Manufacturing Execution Systems Ioannis Danias Continuous Improvement Specialist Linkedin Over the past few years, the pharmaceutical industry has experienced significant advancements in its manufacturing practices, driven by the rapid evolution of Artificial Intelligence (AI) and Machine […]
Can Quality Assurance Benefit Productivity? Can Quality Assurance Benefit Productivity? Nefeli Stylla QA & CSV Specialist Linkedin Quality Assurance: Is it really just a necessary Evil? Quality assurance (QA) is regarded by many as a necessary evil— vital for ensuring quality and compliance but accompanied by procedures and resource demands that constrain productivity. While these […]
