Root Cause Analysis and CAPA Training

Master Root Cause Analysis & CAPA – Register Now!

Are you a pharmaceutical professional looking to enhance your investigative skills and compliance expertise?

Join our upcoming “Root Cause Analysis & CAPA” training—designed to equip professionals with the essential tools needed to achieve operational excellence, regulatory compliance, and quality assurance in the pharmaceutical industry.

🔎 Why Attend This Training?

Pharmaceutical companies face non-conformance issues, audit findings, and compliance risks that can lead to recurring failures and compromised product integrity.

This specialized one-day training will provide you with:

✅ A structured approach to Root Cause Analysis (RCA) for identifying and resolving issues effectively.

✅ Insights into CAPA (Corrective and Preventive Actions) to enhance compliance and prevent recurrence.

✅ Practical knowledge on event detection, deviation management, and risk assessment tools.

✅ Regulatory guidance from industry experts with extensive experience in FDA, EU, WHO, HC, and MHRA GMP/GSDP regulations.

🎯 Who Should Attend?

This training is ideal for professionals in:

•Regulatory Affairs

•Quality Assurance & Control

•Pharmaceutical Manufacturing & Storage

•Auditing & Compliance

•Risk Management in Pharma

👩‍🏫 Meet the Trainer: Dr. Nadia ARA Ghazal

Dr. Ghazal holds a Ph.D. in Pharmaceutical Technology and a Master’s in Biotechnology from the UK, with 34+ years of experience in pharmaceutical manufacturing, quality control, and compliance.

She has worked with FDA, EU, WHO, HC, and MHRA GMP/GSDP regulations, making her an industry leader in regulatory compliance.

📅 Training Details

📌 Date: 27th February 2025

⏰ Time: 9:00 AM – 5:00 PM (Jordan Time)

🌍 Location: Online (via Microsoft Teams)

💲 Fee: $300 per participant (10% discount for groups of 2+ from the same company)

📖 Course Agenda

📌 RCA Definitions & Regulatory Requirements

📌 Deviation Management & Documentation

📌 Root Cause Investigation & Analysis Tools

📌 CAPA Implementation Throughout the Product Lifecycle

📌 Risk Assessment (FMEA) & Case Studies

📌 CAPA Action Plan & Effectiveness Checks

📝 How to Register?

👉 Secure your spot now: REGISTER HERE

📞 Contact for Registration Help:

📱 +966 552830502 | +971 555255081

📧 info@careicon.com.sa | sales@lavida-pharma.com

🌐 www.careicon.com.sa

Take this exclusive opportunity to enhance your expertise and ensure compliance with global pharmaceutical standards. Register today! 🚀