Opportunities lie in enhancing data integrity auditing skills within pharmaceutical manufacturing, focusing on GxP audits. Companies can capitalize by offering comprehensive training that delves into ...
This guide explores how regulated laboratories can achieve strong data integrity by digitalizing key processes ...
Market growth underscores rising demand for data integrity, automation, and compliance-ready digital platforms across global pharmaceutical operationsDelray Beach, FL, Jan. 27, 2026 (GLOBE NEWSWIRE) - ...
Built-in data integrity is a bare minimum requirement in today’s BioPharmaceutical manufacturing. Good Manufacturing Practices (GMP) regulations of the Food and Drug Administration (FDA) highlight the ...
Strengthen information governance with clear policies for data classification, retention, and legal holds to meet industry regulations and ensure defensibility. Embed compliance and collaboration ...
Microbial testing, analysis and environmental monitoring is fundamental to safe pharmaceutical manufacturing. Regulatory agencies require that the many components of the system implemented, from ...
Anton Paar has introduced a new measurement system for pharmaceutical quality control that sets the highest standards in ...
Microbial testing, analysis and environmental monitoring is fundamental to safe pharmaceutical manufacturing. Regulatory agencies require that the many components of the system implemented, from ...