Dublin, Nov. 07, 2025 (GLOBE NEWSWIRE) -- The "Computerized Systems Validation, Data Integrity & Cloud Computing In Pharma & Biotech (Dec 9th - Dec 10th, 2025)" training has been added to ...

The use of computer systems in medical device manufacturing has rapidly expanded, creating a growing need for modernized ...

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 ...

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

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation (CSV) Training Course (Sept 23rd - Sept 25th, 2025)" training has been added to ResearchAndMarkets.com's offering. The attendee will learn ...

"Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities" training has been added to ResearchAndMarkets.com's offering.

The study makes clear that regulators expect human oversight to remain central to pharmaceutical quality assurance. Human operators must participate at key control points and retain authority to ...

Biopharma manufacturers who want to validate their cloud-based biomanufacturing systems can’t apply the same processes to the cloud that they apply to their on-premises computer systems. Cloud ...

"You are only as strong as your weakest link." I cannot think of a better proverb when it comes to surviving in an industry as regulated and as nerve-wracking as pharmaceuticals or life sciences. One ...

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