MasterControl Manufacturing Excellence (Mx) ranked No. 7 on G2's 2026 Best ERP Software list—recognition earned through verified customer reviews. Discover why life sciences manufacturers choose Mx to eliminate production errors, accelerate time to market by 70%, and deliver seamless ERP integration.
Struggling with manual compliance processes? Discover how AI-enhanced quality management systems are helping pharma manufacturers achieve 100% FDA and ISO compliance—without disrupting operations or breaking budgets. Learn practical strategies for transforming compliance from burden to competitive advantage.
The focus has shifted from compliance to operational agility in medical device manufacturing. Four forces are reshaping the industry’s landscape: supply chain regionalization, digital thread mandates, embedded AI, and workforce transformation. Discover how leaders are turning industry changes into competitive advantages.
Digital compliance processes are now competitive differentiators for CDMOs striving to win sponsor contracts. Yet recent data reveals a surprising gap: only 27% of CDMOs have implemented electronic batch records. Discover what sponsors really want and the strategic moves that put contract manufacturing leaders ahead.
Cell and gene therapies are revolutionizing medicine, yet most manufacturers still rely on paper-based processes that can't scale. Discover why digital transformation is essential for CGT success and how to build the right foundation for your operation.
Quality leaders are facing unprecedented change: AI moving from pilot to production, CSA becoming regulatory reality, and inspection-anytime expectations. Learn about these and the other key trends reshaping pharma quality and how to navigate them with confidence.
February 5, 2026
by Betsy Rogers, Senior Product Manager, AI/ML, MasterControl
Managing SOP compliance is increasingly time-consuming, manual, and reactive for quality teams operating in regulated environments. Learn how the new AI-powered SOP Analyzer tool helps identify compliance gaps faster, reduces review burdens, and supports audit readiness.
February 4, 2026
by Jake Ure, Sr. Product Manager, MasterControl
Your QA teams are buried in manual batch reviews while patients wait for therapies. Discover how digital batch disposition transforms this critical bottleneck into a strategic advantage—with practical principles from BioPhorum’s Batch Disposition Manifesto and actionable steps any organization can implement today.
According to LNS Research's independent analysis, MasterControl ranks No. 1 in Growth Potential among Enterprise Quality Management Software (EQMS) vendors. Learn what sets the data-first platform apart and how to select the right quality management solution for your organization.
Most AI initiatives stall at the pilot phase. Discover the AI trends transforming life sciences manufacturing in 2026—from specialized workforce copilots to computer vision achieving 99% accuracy in quality operations.
Life sciences manufacturers are slashing unplanned downtime by 50% with AI-driven predictive maintenance. Explore this and the other critical trends transforming asset management from a reactive cost center into a strategic competitive advantage.
Stuck between basic EBR systems that don't do enough and expensive MES platforms that do too much? Most pharma manufacturers are trapped in this uncomfortable middle ground, struggling with data silos, higher error rates, and systems that can't keep up with modern production demands. Discover the emerging solution category that's helping pharma manufacturers bridge this gap and get an evaluation framework to choose the right fit for you.
MasterControl has been named the No. 1 MES and No. 1 QMS on G2 for Winter 2026—recognition earned entirely through verified customer reviews. Manufacturing and quality teams report measurable results: faster audit inspections, reduced manual errors, seamless operational execution, and audit-ready compliance without compromise. Discover why your industry peers rated MasterControl solutions the best for usability, support, and user adoption.
Zero CDMOs have achieved full digital integration with sponsors, yet 92% report sponsors are raising digital requirements in negotiations. The window between "nice to have" and "deal-breaker" is closing fast. In this exclusive MasterControl-PharmaSource survey of 50-plus global CDMOs, discover why nearly three fourths of contract manufacturers struggle with digital transformation, which AI applications show the biggest impact vs. implementation gap, and what separates digital leaders from laggards.
The era of incremental digital change in the medical device industry is over. Digital transformation is now a regulatory mandate, with five intersecting trends reshaping quality management in the industry. From the QMSR go-live to AI governance frameworks and the "inspection-anytime" reality, quality leaders face an unprecedented convergence of compliance pressures. Discover the most critical trends demanding your attention now and learn why a connected quality ecosystem is no longer optional.
MasterControl has earned the 2026 TrustRadius Buyer's Choice Award, a recognition based on verified customer reviews rating us best in capabilities, value for price, and customer relationships. Learn how life sciences professionals are achieving big efficiency gains, eliminating paper-based processes, and maintaining compliance without complexity through our award-winning quality and manufacturing solutions. Read authentic customer testimonials revealing measurable results—from reducing batch record creation time by 70% to consolidating hundreds of SKUs into optimized digital workflows.
In the medical device industry, the data is clear: physician trust drives prescribing behavior, accelerates market adoption, and protects market share during competitive pressure. Are you building trust or losing ground? Learn how what manufacturers can do to gain physician confidence in their medical devices.
The life sciences landscape is rapidly converging, making isolated systems a relic of the past. Are you ready for the intelligent operations of 2026? This post dives into the three powerful forces that are fundamentally rewiring how pharma and med device companies thrive. Discover why a connected foundation is non-negotiable for compliance, innovation, and empowering your workforce.
The FDA's transition to the QMSR is creating a turning point for CDMOs in the medical device industry. Traditional quality systems can't keep pace with complexity, but AI offers a transformative solution. Discover how AI-powered quality management helps CDMOs navigate QMSR and ISO 13485 compliance and turn regulatory challenges into a competitive advantage.
Unlock physician trust! This blog post reveals how transparent data is now critical for pharma manufacturers. Beyond compliance, digital solutions transform operational insights into verifiable evidence of quality, building physician confidence and a competitive edge. Dive in to understand why data visibility is the ultimate trust imperative in the evolving health care landscape.
