This training unlocks opportunities for companies to modernize GxP validation by shifting to Computer Software Assurance, ensuring data integrity and compliance with FDA regulations, and addressing ...

CARY, N.C., Dec. 16, 2025 /PRNewswire/ -- InstantGMP™, a provider of cloud-based GMP and FDA compliance software for pharmaceutical and other regulated manufacturers, announced it has aligned its ...

(MENAFN- EIN Presswire) EINPresswire/ -- InstantGMPTM, a provider of cloud-based GMP and FDA compliance software for pharmaceutical and other regulated manufacturers, announced it has aligned its ...

InstantGMP categorizes software functions into low, moderate, and high process-risk groups. Low-risk features, such as equipment, room, deviation, and CAPA logs, primarily collect or tabulate data.

For more than 15 years, Aldo Vidinha has worked at the intersection of engineering, quality, and regulatory strategy in the life sciences. His career has taken him across Europe, Asia, the United ...

BrainSpace announced that the FDA granted 510(k) clearance for its Intellidrop automated brain fluid management system.

Here are 40 spine devices and technologies earning FDA clearances in 2025. Note: This is not an exhaustive list. 1. SurGenTec earned FDA 510(k) clearance for its OsteoFlo HydroFiber to be used as a ...

QualityKiosk Technologies, a global leader in digital assurance and reliability engineering solutions, is proud to announce its strategic partnership with DevRev, an AI-native enterprise software ...

The US Food and Drug Administration on Monday approved a daily pill version of Novo Nordisk’s weight-loss drug Wegovy, introducing a new option for how patients can take medicines in a class of drugs ...

PRINCETON, N.J.--(BUSINESS WIRE)--QualityKiosk Technologies, a global leader in digital assurance and reliability engineering solutions, is proud to announce its strategic partnership with DevRev, an ...