When: Available on demand. (Original presentation date: March 2019)
Overview
This course provides an overview of medical device regulations in Jordan, from classifications to procedures for access to the market and lifecycle management. The webinar will also address labelling requirements, advertising and pharmacovigilance.
Learning objectives
- Definition and classification of medical devices in Jordan
- Approval procedures, requirements and timelines for different types of medical devices
- Lifecycle management of medical devices including labelling, advertising and pharmacovigilance requirements
Target audience
Regulatory professionals who would like an overview of the regulatory framework for Medical Devices Jordan.
Presenter
Anan Abu Hassan
Anan has been a Consultant at veronica pharma for pharmaceutical consultations since September 2018, prior to this she was the Director Assistant of Medical Devices and Cosmetics Directorate at JFDA. Anan has worked in various roles in medical devices and cosmetics and was also Head and member in different technical committees at JFDA such as: Cosmetics technical committee, Medical devices technical committee, Quality control committee, Primary classification committee, Single window committee and Risk management unit.
CPD
This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
How do I register?
Prices
| Type |
Member |
Non-member |
| Standard |
£70 + VAT |
£95 + VAT |
Discounted Places
A limited number of discounted places are available at the rates below for those:
Please email meetings@topra.org for a discount code before making your booking.
| Type |
Member |
Non-member |
| Discount |
£35 + VAT* |
£47.50 + VAT* |
* VAT, if applicable, is charged at a rate of 20%.
Terms and conditions
Please read the training terms and conditions before booking this webinar. By booking this webinar, you are agreeing to the terms and conditions.