Market opportunities arise from the growing need for modernization and compliance assurance in FDA-regulated industries focusing on data integrity. Emphasizing cloud computing, automation, and mobile ...

LIMERICK, Ireland, Oct. 08, 2024 (GLOBE NEWSWIRE) -- kneat.com (KSI:CA), inc. (OTC: KSIOF), a leader in digitizing validation and quality processes, is pleased to announce that a global pharmaceutical ...

The market opportunities lie in leveraging data process mapping to enhance data integrity and regulatory compliance, particularly aligning with FDA standards. There's potential in addressing gaps, ...

Market opportunities lie in modernizing software development and validation approaches, emphasizing agility and continuous validation to meet changing needs, while ensuring compliance with FDA ...

Unicon Pharma, a leading provider of compliance, validation, and workforce solutions for the life sciences industry, announced a strategic partnership with VRR Life Sciences, a Bangalore, India-based ...

Microbial testing, analysis and environmental monitoring is fundamental to safe pharmaceutical manufacturing. Regulatory agencies require that the many components of the system implemented, from ...

Please give an overview of the recent compliance pressures that have been put on pharmaceutical companies. Compliance always has always been a high priority for data integrity in the pharmaceutical ...

Bryan Ennis is the CEO and cofounder of Sware, a regulatory technology company serving healthcare, life sciences and SaMD companies. “The measure of intelligence is the ability to change.” This famous ...

Dublin, May 14, 2025 (GLOBE NEWSWIRE) -- The "Risk-based Computer System Validation; Reduce Costs and Avoid 483s (ONLINE EVENT: August 6-7, 2025)" has been added to ResearchAndMarkets.com's offering.

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation for Cloud and COTS Applications-Live Online Training" training has been added to ResearchAndMarkets.com's offering. Advancements in technology ...

Microbial testing, analysis and environmental monitoring is fundamental to safe pharmaceutical manufacturing. Regulatory agencies require that the many components of the system implemented, from ...