The pharmaceutical industry’s approach to data integrity has been historically manual, leveraging physical documentation and potentially unreliable paper-based ...
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 ...
The present world of digital transformation, streamlining workflows, enhancing operational efficiencies, and eliminating paper demands connected workflows with fully integrated systems and equipment.
The "Data Integrity Auditor Masterclass Training Course (Oct 15th-16th, 2025)" has been added to ResearchAndMarkets.com's offering. Data integrity has received more attention than ever before in the ...
In India, pharmaceutical education is developing rapidly, entering in a new digital era. As the sector embraces automation, ...
Hosted on MSN
Glenmark Pharma's North Carolina facility gets 5 USFDA observations; no data integrity issues
Glenmark Pharmaceuticals Ltd on Wednesday informed bourses that the United States Food and Drug Administration (USFDA) conducted a Good Manufacturing Practice (GMP) inspection at its manufacturing ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback