Corrective And Preventive Actions (CAPA) - Online Live Training (Hebrew)
Sun, 11 Feb
|Virtual Event
Corrective and Preventive Actions (CAPA) are the heart of any quality management system (QMS). Learn essential tools and techniques to identify, investigate, and prevent quality issues within your organization. Elevate your skills and drive excellence in every aspect of your business.
Time & Location
11 Feb 2024, 9:30 am – 1:00 pm GMT+2
Virtual Event
About the event
Corrective and Preventive Actions (CAPA) are the heart of any quality management system (QMS). CAPAs are used to identify and address the root causes of problems, and to prevent them from recurring.
By implementing effective CAPA processes, organizations can improve their products and processes, and ultimately, their bottom line.
Training content:
- The purpose of CAPA
- Inputs to the CAPA process
- The steps involved in implementing a CAPA
- The tools and techniques used for root cause analysis
- Risk Assessment
- The importance of monitoring and evaluating CAPAs
The training includes examples from the industry of how companies have implemented successful CAPA programs.
Intended for: All employees involved in the CAPA process.
Training Agenda:
09:30 – 10:00 Introduction to CAPA: Overview and Regulatory Requirements
10:00 – 11:30 Requirements of the following CAPA elements:
- Problem Description (including Risk Assessment)
- Containment Action/s
- Investigation and Root Cause Analysis Tools
11:30 - 11:45 Break
11:45 – 12:30 Requirements of the following CAPA elements:
- Corrective Actions and Preventive Actions
- Effectiveness Verification
Monitoring and escalations of CAPA's
12:30-13:00 Q&A
About the trainer:
Helit Dovrin - Executive Consultant, Coach, Auditor and Lecturer worked for more than 25 years as Quality and Regulatory Senior Leader at the world leading medical device companies such as: Philips Healthcare, GE Healthcare, Align Technology and Biosense Webster part of Johnson & Johnson.
Helit gained experience & expertise in all areas of the Quality Management System and Regulatory Affairs including FDA & Notified Body Inspection Management, ISO-13485, EUMDR & MDSAP Compliance Audits, and Quality & Safety escalations.
Tickets
General Ticket
₪350.00Sale ended
Total
₪0.00