A) WHO SHOULD ATTEND THE WORKSHOP:

All healthcare professionals in liberal positions (Physician, Pharmacist, Nurse, Pharmacy Preparers, Midwives, etc) who wish to deepen their knowledge of the field of patient safety for better advice and better management of adverse effects/events.

B) OBJECTIVES FOR PARTICIPANTS:

• Acquire the new requirements of the Algerian and international regulations (FDA, EMA, HC, SFDA…)
• Recognize and manage adverse events and product quality complaints
• Electronic patient record in pharmacy 4.0 to improve quality and patient safety
• The involvement of IT (Information Technology), digitalization and artificial intelligence solutions in the automatic detection of adverse events and their management.

C) CONTENT:

• General information on pharmacovigilance (definition and classification of adverse events)
• Why, what and how to report adverse events
• Patient record / collection of information
• Pharmacy 4.0: perspective in patient safety
• Practical Examples – Questions – Answers
• Workshop with Quiz: An Example of the Canadian Model and Case Studies

HOURLY VOLUME:

• General notions
• Regulation
• Pharmacoepidemiology
• Data management
• A 3-hour module with a coffee break
• A 1-hour workshop with questions and answers

E) THE 50,000 D.A PACKAGE INCLUDES:

• Coffee break
• Educational support
• Training certificate
• Free 20-minute personal consultation and networking session on Pharma business opportunities in North America.