2022-11-17 2022-11-17 , online online, 1.090,- € zzgl. MwSt. Ala'a Saleem https://www.forum-institut.de/seminarDetail/818/referenten/22/22_11/22112502-online-course-marketing-authorisation-mena-medical-devices_saleem-alaa.jpg Marketing Authorisation of Medical Devices in Saudi Arabia, the UAE and Jordan

Medical Devices: Marketing authorisation and market access in Saudi Arabia, the UAE and Jordan. Don't miss out on this unique course! First-hand information provided by experienced speakers to guarantee market success of your enterprise.

Topics
  • MENA as a market: The economy, people and culture in the Middle East
  • EU Medical Device Regulation: Effects on the MENA region
  • The regulatory framework for marketing authorisation in Saudi Arabia, the UAE and Jordan
  • Crucial changes to the regulatory requirements
  • Post-market requirements
Aims and objectives
The Middle East and North Africa (MENA) region is one of the last untapped but relevant growth regions for pharmaceutical and healthcare companies. The markets are highly regulated and challenging in terms of economic policy, but they are worth the effort. The United Arab Emirates (UAE) are expected to grow by 8% until 2024, and the Kingdom of Saudi Arabia by almost 6%.

In this online seminar, you will learn about the regulatory framework and its most important changes for Saudi Arabia, the UAE and Jordan. In addition, our experts will address the impact of the EU MDR on the MENA region.

Successful and sustainable entry into the MENA region requires openness and understanding of Arab (business) culture. Our local speakers will outline the most important aspects of the economy, people and culture in the Middle East, ensuring that nothing stands in the way of successful market entry for you!
Who should attend

This unique course addresses the needs of professionals in the medical device industry involved in registering, exporting and manufacturing medical devices in the Middle East.

In particular, members of the following departments will benefit from the speakers' expertise:

  • Business Development;
  • Regulatory Affairs;
  • Market Access; and
  • Export.

Please note: If there are not enough participants, the event will be cancelled 3 weeks in advance. Therefore, please register in good time!

Medical Devices in the Middle East & North Africa (MENA)

Marketing Authorisation of Medical Devices in Saudi Arabia, the UAE and Jordan

Successful market entry in the MENA region.

Benefits
  • Excellent speakers from the MENA region
  • All neccessary information in one day
  • We are following the IMI quality criteria

Webcode 22112502

Jetzt buchen

JETZT Buchen

Referenten


Alles auf einen Blick

Termin

17.11.2022

17.11.2022

Zeitraum

9:00 -17:00

9:00 -17:00
Veranstaltungsort

online

online

Gebühr
Ihr Ansprechpartner

Antje Bauer
Conference Manager

+49 6221 500-655
a.bauer@forum-institut.de

Details

Medical Devices: Marketing authorisation and market access in Saudi Arabia, the UAE and Jordan. Don't miss out on this unique course! First-hand information provided by experienced speakers to guarantee market success of your enterprise.

Topics
  • MENA as a market: The economy, people and culture in the Middle East
  • EU Medical Device Regulation: Effects on the MENA region
  • The regulatory framework for marketing authorisation in Saudi Arabia, the UAE and Jordan
  • Crucial changes to the regulatory requirements
  • Post-market requirements
Aims and objectives

The Middle East and North Africa (MENA) region is one of the last untapped but relevant growth regions for pharmaceutical and healthcare companies. The markets are highly regulated and challenging in terms of economic policy, but they are worth the effort. The United Arab Emirates (UAE) are expected to grow by 8% until 2024, and the Kingdom of Saudi Arabia by almost 6%.

In this online seminar, you will learn about the regulatory framework and its most important changes for Saudi Arabia, the UAE and Jordan. In addition, our experts will address the impact of the EU MDR on the MENA region.

Successful and sustainable entry into the MENA region requires openness and understanding of Arab (business) culture. Our local speakers will outline the most important aspects of the economy, people and culture in the Middle East, ensuring that nothing stands in the way of successful market entry for you!

Who should attend

This unique course addresses the needs of professionals in the medical device industry involved in registering, exporting and manufacturing medical devices in the Middle East.

In particular, members of the following departments will benefit from the speakers' expertise:

  • Business Development;
  • Regulatory Affairs;
  • Market Access; and
  • Export.

Please note: If there are not enough participants, the event will be cancelled 3 weeks in advance. Therefore, please register in good time!

Detailed programme

9:00 -17:00

Market Entry in MENA
  • Overview of the markets, economy, people and culture in the Middle East
  • Product dependent regulatory framework
  • Building regulatory strategy for MENA
  • Legal considerations for agents and distributors
  • Specifics of marketing channels, pricing and reimbursement

How EU MDR affects MENA
  • Highlighting relevant MDR changes
  • Aspects of MDR change on MENA

Marketing authorisation in Saudi Arabia
  • Regulatory framework
  • Crucial changes to the regulatory requirements
  • Authorised representative: Setup and implications
  • Required documents, the registration process and maintenance
  • Post-market requirements

Marketing authorisation in the UAE
  • Regulatory framework
  • Crucial changes to the regulatory requirements
  • Required documents, the registration process and maintenance
  • Post-market requirements

Marketing authorisation in Jordan
  • Regulatory framework
  • Marketing authorisation procedure and requirements
  • Post-approval activities

Q&A session with our experts


Good to know

Your take-aways

  • First-hand information provided by local speakers
  • Enough time for questions and discussion
  • Focus on medical devices
  • Marketing authorisation and market access in a single course

How does an online seminar work?

Our online training courses are live and interactive. They are held and controlled directly by our speaker. You may take part in the seminar from anywhere using your end device. You will see the presentation and listen to our speaker's lecture using Internet telephony (VoIP) or even a normal telephone connection. And you can also ask questions live.

1. You will receive brief instructions on how to use Zoom beforehand.
2. 48 hours before the online seminar, you will receive an email with an access link and a meeting ID.
3. Use a headset, loudspeakers or the telephone for audio.
4. Listen to the speaker and follow the presentation.
5. Feel free to switch from silent to audio mode by yourself any time to ask your questions.

What are the advantages of our online courses?

  • Online courses - live and interactive via Zoom.
  • Your access data and all accompanying documents always accessible in your customer portal.
  • Didactically and technically optimally coordinated concept with plenty of room for your questions.
  • Free PreMeeting for a technically perfect start to your online training.
  • Continuous support during the online seminar for optimal learning success.

FAQs

1) What are the system requirements?
You need a stable internet connection. The following browsers are possible under Windows, for example:
  • - Internet Explorer version 8.0 or higher
  • - Mozilla Firefox
  • - Google Chrome

For participation via mobile devices, we recommend the Zoom app. You will need a headset, loudspeaker or telephone to transmit the sound.
For more information, please visit: Zoom Support

2) Can I do a technology check in advance?
You can carry out a technology check in advance to ensure that everything works at the actual online seminar.
The technology check can be carried out at: Zoom Test

3) Do I have to use a PC headset for the online seminar?
No, Zoom supports dial-in via telephone in addition to all standard PC microphones or speakers. However, working with a PC headset is much more comfortable for online seminars.

This distinguishes our events

Overall score of all evaluations in 2021

Five stars on Trustpilot = Excellent

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Technical requirements

Here you can find the technical requirements for our online events that must be met.

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Technical requirements
List of abbreviations

Your free guide through the jungle of abbreviations as to regulatory issues. Download the list for free.

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Abbreviations, Glossary
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