The US FDA has issued a Form 483 to Dabur India following an inspection of its Dadra and Nagar Haveli plant. Discover the ...

A Form 483 is issued at the conclusion of an FDA inspection when investigators observe conditions that may violate US drug manufacturing regulations.

The company helps manufacturers automate inspection, counting, and quality control with AI-enabled machine vision and edge automation ...

Misumi Americas merges Fictiv digital platform with precision manufacturing backed by $1 billion investment and new American ...

Robotic CNC machine tending is becoming more flexible as leading suppliers bring new software and integration to industry.

The FDA has flagged serious data integrity and manufacturing issues at Dabur India's plant, emphasizing microbiological ...

Dabur India has come under intense regulatory scrutiny after investigators from the U.S. Food and Drug Administration (USFDA) documented a series of significant quality, data ...

As high-NA EUV approaches, mask makers need new metrics, model-based checks, and curvilinear-native data flows to keep turn ...

Global pharmaceutical major Lupin Limited has announced that it has received the Establishment Inspection Report (EIR) from the United States Food and Drug Administration (USFDA) for ...

ViewTech Borescopes, a leading provider of remote visual inspection (RVI) equipment, will exhibit at the 2026 Space Tech Expo USA, taking place ...

Achieve Life Sciences, Inc., a late-stage specialty pharmaceutical company focused on the global development and ...