Original presentation date: March 2019
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.
- 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
Regulatory professionals who would like an overview of the regulatory framework for Medical Devices Jordan.
Anan Abu Hassan 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.
This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.
Once you have paid for the webinar, you will receive an email from email@example.com with a link to the webinar within one hour. Once received, simply click on the link in the email to access the webinar. You will have access to the webinar for six months from the day of purchase.
Please note, if you select the pay later option, you will not have access until payment has been cleared.
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.
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