Click to read RCA's regulatory compliance consultants give best practices regarding requirements for technology transfer in pharma.
Join Dr. Steven Coulter as he addresses the question, Are Risk Management and Design Controls two different processes?
Learn more about CDER's Quality Management Maturity program & how manufacturers can develop compliant processes that promote improvement.
Click to read RCA's regulatory compliance consultants describe how virtual audit training has positively impacted FDA inspection success.
Click to read RCA’s medical device consultant analysis of clinical evaluation regulations for medical devices under FDA & EU’s MDR.
Click to watch RCA's Seyed Khorashahi during our webinar discuss a medical device inspection & types of innovative preparation strategies.
Click to learn from RCA's pharmaceutical consultants as they discuss ALCOA and Data Integrity elements to avoid FDA regulatory citations.