CenPharma has been contracted to write the Quality Manual for a clinical phase start up (as well as the Quality statement and their procedures for the use of AI). This is one of our core services.
The Quality Manual can be a nuanced undertaking depending on phase, modality and outsourced manufacturing and testing (if applicable)
Does your firm need a Quality Manual written, tweaked, reviewed or revised?
Reach out to one of our experts at info@cenpharma.com
CenPharma is a pharmaceutical consulting firm specializing in compliance, engineering and technical services. We specialize in designing and implementing systems in diverse areas such as method design, method transfer, quality compliance, quality assurance, inspection readiness, process validation, analytical method validation, equipment qualification, facility design, supplier qualification, environmental monitoring, quality management systems, learning management systems, materials management, auditing (hosting and conducting), compliance remediation, quality systems, investigation, root cause analysis, technical writing, change management, data integrity and quality control. Our team consists of experience pharmaceutical industry professionals with expertise in microbiology, engineering, compliance, system design and regulatory affairs.
This post is related to:
Stay informed on pharmacy supply chain news, market trends, and product releases by subscribing to RXinsider’s emails, newsletters, and publications. If building awareness with pharmacy management is part of your marketing strategy, consider advertising with RXinsider.
