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CGMP: Pharmaceutical CAPAs (GMP10)

Duration : 90 Minutes

Kelly Thomas,

Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation,  21 CFR Part 1 Read more


This online training program describes corrective and preventive actions (CAPAs), and how good manufacturing practices can be applied to eliminate causes of non-conformities or other undesirable situations. The training program enables the students to interpret and identify the requirements of a pharmaceutical CAPA system.

As a fundamental management tool, CAPA is integral to the effectiveness of a quality management system. The objectives of this course are to teach the requirements of ICH Q10- PQS (Pharmaceutical Quality System), describe escalation and tracking processes in a CAPA system, explain the importance of investigation and risk assessment, list a CAPA system's critical elements, explore the different processes and phases of a good CAPA system, and identify a CAPA system's regulatory requirements.

Course Objectives:

• Identify the regulatory requirements for a CAPA system.
• List the various phases and the processes of a successful CAPA system.
• Explain the critical elements of a CAPA system.
• Explain the importance of risk assessment and investigation.
• Describe tracking and escalation processes in a CAPA system.
• Recognize the requirements of ICH Q10 - Pharmaceutical Quality System (PQS).

Course Outline:

INTRODUCTION

• Introduction
• Overview
• Pharmaceutical Quality System (PQS) Model
• Key areas of the QMS
• Reviews and assessments
 
REGULATIONS

• Overview
• Compliant CAPA systems
• Activity: Looking for CAPA requirements within GMPs
• FDA QSIT inspections of CAPA systems
• Important definitions
• Examples of different CAPAs
• Topic review
 
THE CAPA SYSTEM

• Overview
• Features of a CAPA system
• CAPA flowchart
• Phases of a CAPA system
• Topic review
 
ELEMENTS OF CAPA SYSTEMS

• Overview
• CAPA system inputs
• Risk assessment and CAPA
• Risk assessment process
• CAPA documentation
• The CAPA procedure
• CAPA request/record
• Correction/containment
• Corrective action
• Preventive action
• Verification and closeout
• Completed CAPA report
• Topic review
 
ROOT CAUSE ANALYSIS

• Symptom or Root Cause?
• When to conduct RCA/CAPA
• Root Cause Analysis (RCA)
• Investigation & Analysis
 
TRACKING AND ESCALATION

• Overview
• Progress tracking and escalation
• CAPA trending
• Topic review
• Summary

What You Get:

• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points

Who Will Benefit:

• Production personnel
• QA/QC personnel
• R&D managers
• Compliance officers
• Executive managers
• Risk management specialists
• Manufacturing Personnel & Management
• Senior Management
• Regulatory Affairs Personnel & Management
• Quality Assurance Personnel & Management
• Drug development companies

Please reach us at 1-888-844-8963 for any further assistance or if you wish to register

100% MONEY BACK GUARANTEED

Refund / Cancellation policy

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Subject : CGMP: Pharmaceutical CAPAs (GMP10)


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