Explore a wealth of knowledge designed to inform, inspire, and support your journey. Start exploring today! Search by type - Any - Blog Customer story Event News White paper - Any -BlogCustomer storyEventNewsWhite paper August 7, 2026 Cognex In-Sight 5000 Obsolescence: Five Questions to Answer Before Your Machine Vision Upgrade The Cognex In-Sight 5000 Series is obsolete, but replacing it involves much more than swapping cameras. Discover the five key questions every manufacturer should answer before upgrading their machine vision system. Blog Read more August 7, 2026 Self-Healing AI: A Paradigm Shift for Regulated Manufacturing Discover how self-healing AI is reshaping regulated manufacturing. By continuously adapting, retraining, and staying compliant, it turns production into a smarter, more resilient, and audit-ready process—paving the way for the Factory of the Future. Blog Read more July 31, 2026 The EU AI Act: What Does It Mean for Pharmaceutical Inspection? The EU AI Act is reshaping how artificial intelligence is developed and deployed across regulated industries. Discover what pharmaceutical manufacturers need to know about AI-powered inspection, including validation, transparency, traceability and maintaining GMP compliance. Blog Read more May 7, 2026 Connecting Legacy Automation to Modern GMP Operations Modern digital manufacturing starts with connected systems. Explore how life sciences manufacturers are integrating legacy infrastructure with modern digital operations to improve visibility, efficiency, and compliance. Blog More on connecting legacy automation March 10, 2026 SOP audit: what inspectors look for The standard operating procedure (SOP) for line clearance is frequently scrutinized because it represents a primary control against cross-contamination and mislabeling. Blog More on SOP audits March 9, 2026 Reducing downtime and increasing productivity The requirement for rigorous safety checks often creates a tension between the need for speed and the necessity of quality. Blog More on reducing downtime during line clearance March 8, 2026 The hidden cost of manual line clearance in pharma manufacturing Many manufacturers rely on manual visual inspections by operators, this approach carries significant financial and operational risks that are not always immediately visible on a balance sheet. Blog More on hidden costs of manual line clearance March 7, 2026 Creating effective SOPs for line clearance As production environments become more complex traditional paper-based SOPs for line clearance often fall short of their intended goal due to their static nature. Blog More on effective SOP's for line clearance March 6, 2026 Complying with cGMP, GMP, 21 CFR Part 11 and annex 11 guidelines Maintaining compliance during line clearance is not just a matter of operational preference but a legal requirement that determines a facility's right to operate. Blog More on compliance during line clearance March 5, 2026 Automation and the role of machine vision As production speeds increase and regulatory requirements become more stringent, the limitations of manual inspection are becoming more apparent Blog More on line clearance automation January 29, 2026 Delivering Value: Aligning KPIs and Quality for Real Impact In this third instalment of our Ask the Expert series, Mike explains how Catalyx keeps delivery tightly aligned with client KPIs, ensuring that every action drives tangible, data-backed outcomes. Blog Read more January 22, 2026 Smarter Scaling for Pharma’s Real-World Challenges This is Part 2 of our three-part ‘Ask the Expert’ series with Mike, Director of Sales and Delivery at Catalyx, where we uncover what makes their non-conventional outsourcing models so effective in the pharmaceutical industry. Blog Read more Pagination Current page 1 Page 2 Page 3 Next page ›› Last page Last » Your vision+ our expertise= your success! Let's invent together