Pharmacovigilance

• We introduce this course for pharmacists and all health care providers, which will support all of them with updated knowledge about pharmacovigilance after careful consideration of the scientific and medical knowledge. It is designed to cover all aspects of Pharmacovigilance and drug safety management. This course is based on the European guideline on GVP, WHO and is a complete training solution for all individuals that need to acquire pharmacovigilance knowledge. Our training can also serve as a refresher course. It is consistent with the legislation changes in EU and is suitable for everyone who needs to be up-to-date with the pharmacovigilance guidelines or is involved in drug safety, pharmacovigilance, regulatory and quality compliance. This course will allow you to enjoy the learning process and easily understand the fundamentals of Good Pharmacovigilance Practice.

• In this section, we will provide in details what is in guidelines about pharmacovigilance definition, legal and ethical background then we will discus pharmacovigilance system, adverse events, the role of the qualified person responsible for pharmacovigilance, detailed description of the pharmacovigilance system, reporting of adverse reactions and risk management.

Pharmacovigilance English
Last update Dec 2019

Overview

• We introduce this course for pharmacists and all health care providers, which will support all of them with updated knowledge about pharmacovigilance after careful consideration of the scientific and medical knowledge. It is designed to cover all aspects of Pharmacovigilance and drug safety management. This course is based on the European guideline on GVP, WHO and is a complete training solution for all individuals that need to acquire pharmacovigilance knowledge. Our training can also serve as a refresher course. It is consistent with the legislation changes in EU and is suitable for everyone who needs to be up-to-date with the pharmacovigilance guidelines or is involved in drug safety, pharmacovigilance, regulatory and quality compliance. This course will allow you to enjoy the learning process and easily understand the fundamentals of Good Pharmacovigilance Practice.

• In this section, we will provide in details what is in guidelines about pharmacovigilance definition, legal and ethical background then we will discus pharmacovigilance system, adverse events, the role of the qualified person responsible for pharmacovigilance, detailed description of the pharmacovigilance system, reporting of adverse reactions and risk management.

This Activity for

  • Other health care provider
  • Respiratory Therapy
  • Psychology
  • Podiatry
  • Physiotherapy
  • Optometry
  • Clinical Nutrition
  • Nursing and Midwifery
  • Dentistry and Related Specialties
  • Resident / Fellow
  • Physician
  • Pharmacy
  • Occupational Therapy
  • Clinical Laboratory Sciences
  • Non Health Care Provider
  • Healthcare & Hospital Administration
  • Health Education
  • Health Informatics
  • Speech-Language Pathology

What I will learn?

1-Being aware with pharmacovigilance.
2-To introduce the principles of good pharmacovigilance practice, the current legal regulations and guidelines
3-Diagnosis and Management of Adverse Drug Reactions
4-The clinical management of adverse reactions
5-To have the confidence to outline the main GVP requirements related to the pharmacovigilance and risk management systems
6-Get familiar with the essential documents related to GVP and understand the essence, purpose and structure of important trial related files such as the pharmacovigilance system master file (PSMF)
7-Provide a high-end training thereby enhancing the employment prospects of the participants.

Main Them

Recorded Programs

Pronciples of Risk management Part 1
Due Date 05/02/2020

Objectives of risk management Part 1
Due Date 05/02/2020

Reducing Risk Part 1
Due Date 05/02/2020

.Exam.
Quiz 5 ( 15 Min )
Due Date  05/01/2020

Lessons 4
On-Demand 3
Exam 1

Overview Part 1
Due Date 05/02/2020

Unsolicited report Part 1
Due Date 05/02/2020

Consumer report Part 1
Due Date 05/02/2020

.Exam.
Quiz 4 ( 15 Min )
Due Date  05/01/2020

Lessons 4
On-Demand 3
Exam 1

Overview Part 1
Due Date 05/02/2020

Severity of AE Part 1
Due Date 05/02/2020

Identifying and reporting Part 1
Due Date 28/02/2024

.Exam.
Quiz 3 ( 15 Min )
Due Date  05/01/2020

Lessons 4
On-Demand 3
Exam 1

Overview Part 1
Due Date 05/02/2020

Inspection Part 1
Due Date 05/02/2020

Grading Part 1
Due Date 05/02/2020

.Exam.
Quiz 2 ( 15 Min )
Due Date  05/01/2020

Lessons 4
On-Demand 3
Exam 1

Overview Part 1
Due Date 05/02/2021

Aims of Pharmacovigilance Part 1
Due Date 05/02/2020

Principles of PV Part 1
Due Date 05/02/2020

.Exam.
Quiz 1 ( 15 Min )
Due Date  05/01/2020

Lessons 4
On-Demand 3
Exam 1

Additional items to the activity

Optional Details Type Fee
Pharmacovigilance Certificate

Accreditation

Certificate Free
VAT 15% Included

About Organizer

Contact the organizer and they will be glad to help!

Virtual Medical Academy

was 0 SAR

Free
0%coupon Discount
  • calendar 11 Jul 2020 to 05 Feb 2021
  • quality Certificate Available
  • cme Pharmacovigilance Certificate - 5 CPD Hours
  • marker On-Demand
  • adjust Access materiel is from 2020-07-11 18:08:00 to 2021-02-05 18:08:00
  • Registration Policy Full Course
  • Completion Role You must attend all the Sessions
  • Refund Policy No Refund
Free