Conduct clinical trials, respond to adverse regulatory inspection findings, build a compliant pharmaceutical quality system or create effective corrective and preventive actions (CAPAs) as part of your remediation plan.
Pharmaceutical Quality System Remediation Projects
Develop an action plan for responding to statements of non-compliance, including warning letters and FDA Form 483s. Incorporate our practical remediation solutions into your overall quality system for long-term, sustainable compliance.
January 15 – 18, 2024
16 hrs VILT, 5 hrs self-paced
January 23 – 25, 2024
12 hrs VILT, 4 hrs self-paced
GMP PQS Lead Auditor (CQI & IRCA Certified Training)
January 29 – February 2, 2024
25 hrs VILT, 15 hrs self-paced
To ensure impartiality, use of NSF management systems consulting services or attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.