GET TO KNOW THE GXP REQUIREMENTS FOR PHARMA MANUFACTURING COMPLIANCE GxP is a shorthand umbrella term for regulated “Good Practice” standards in life sciences. The “x”… Read More
PHARMACEUTICAL AUTOMATION SOLUTIONS SUPPORT TRACEABILITY & COMPLIANCE A pharmaceutical assembly line needs a record of what happened to each part throughout production.… Read More
5 WAYS TO OPTIMIZE PRECISION MATERIAL HANDLING IN TRAY AUTOMATION Molded parts come out of the press in a specific, known position. The orientation and pitch are… Read More
6 POINTERS FOR FDA 21CFR PART 11 COMPLIANCE IN PRESS SIDE AUTOMATION FDA 21CFR Part 11 governs electronic records and electronic signatures. A press side automation… Read More
MANUFACTURING AUTOMATION ROI: WHERE’S THE PROOF? Automation systems come with a generalized promise of efficiency…but if you’re an industry vet,… Read More
WHAT IS DESIGN FOR MANUFACTURABILITY & HOW DOES IT HELP AUTOMATION? Imagine a component that meets every functional requirement in a CAD model. Can it still create… Read More
6 LESSONS OF FULLY INTEGRATED AUTOMATION SYSTEMS FOR MANUFACTURERS At its heart, fully integrated automation systems are an architectural strategy to eliminate… Read More
WHEN DO I CHOOSE CUSTOM AUTOMATION SOLUTIONS OVER STANDARD EQUIPMENT? An off-the-shelf conveyor, robot, or packaging machine is a serviceable solution for numerous… Read More
HOW WE APPROACH END-OF-ARM TOOLING FOR PRESS SIDE AUTOMATION For robots, part handling is only as good as the tool at the end of the arm. That may sound… Read More