PTI - international

Training Overview

Improve Your Ability to:

• Carry out the full range of QA responsibilities effectively and efficiently to create a regulatory compliant manufacturing setting
• Complete internal audits by applying proven, practical auditing techniques and anticipate potential problems and weaknesses 
• Properly investigate deviations and implement Corrective and Preventive Actions (CAPA) to locate, document and solve problems faster
• Conduct Root Cause Analysis (RCA) to identify and address underlying problems
• Prepare for a systems-based drug cGMP or QSIT inspection and avoid FDA trigger points
• Remedy compliance issues by performing OOS and failure investigations
• Utilize a risk-based, science-based approach to establish an efficient QA system
• Implement and maintain an effective change control program to help effectively manage changes without delays
• Conduct batch record reviews to ensure your manufacturing processes are effectively documented

PTi international is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmaceutical education. Participants will receive a maximum of 14 hours (1.4 CEUs) of continuing education credit for full participation in the two-day training. ACPE # 326-000-04-054-L04, Initial release: 07/2006.