Master Regulatory Affairs Updates of the META Region

Description

In this course, we will master the challenges of the regulatory affairs profession worldwide and especially in the META region. The region experienced and still experiences a lot of updates and variations in the guidelines and requirements for practicing regulatory affairs, Pharmacovigilance and pharmaco-economics as well.

The META region, which includes the GCC, Africa, and the Levant, each is of these has its own leader of the region. The leader of the region is a country that follows strictly any one of the globally well-known health authorities

For Example, Saudi Arabia the leader of the GCC region follows strictly FDA of the US, Jordan the leader of the Levant area follows Saudi Arabia, while Tunisia follows the EMA of Europe.

The leader country when it comes to any updated regulations, the others follow, from here came the power of the leader's countries.

So, our key to success in the META region is to keep up to date with the continuously changing regulations in the region, as regulatory affairs professionals we have to have a strategic way of thinking, so keeping up to date with close follow-up on these changing regulations, its implementation timeline and enforcement date are so crucial to preparing in advance always to master the region there.

So this course is to complete the full picture of mastering the whole META region, as you have the basics of all regulatory activities from all of the full courses dealing with the registration, renewal, and variations of both medical devices and pharmaceutical products in each and every country in the META region, so to be the expert, complete it with mastering the updates here to stand out of the crowd.

You will find out updates from now and then as per the implementation of the changes in the region, so please keep an eye on my courses dealing with the updates in the region.

eventually, I would like to thank you all my dear future pharma industry professionals and managers, I wish the best of luck to all of you and a very successful career.

What You Will Learn!

• Master Regulatory Affairs Updates in the META Region
• Manage all regulatory activities updated in the META region
• Be the expert of the regulatory guidelines in the META region
• Keep up to date with the regulatory requirements in the META region

Who Should Attend!

• All levels of pharma industry professionals and fresh graduates

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