x

75% of people globally want unbiased news (Pew Research) but are concerned they're not getting that.

Get balanced coverage with Symby. See how stories are covered across diverse outlets and spot when one side covers a story the other skips.

PODCAST

MENA MedTech Insights

Welcome to MENA MedTech Insights, the definitive podcast for professionals in the Middle East and North Africa"s rapidly growing medical technology sector. Each episode, we explore the latest innovations, market trends, and regulatory landscapes, featuring exclusive interviews with the founders, investors, and leaders who are shaping the future of healthcare in the region.

science life sciences

All Episodes

03:12

Navigating Kuwait's MedTech Maze: Does MDSAP...

MENA MedTech Insights ·

2025/08/30

The Medical Device Single Audit Program (MDSAP) simplifies access to major global markets, but its acceptance in the MENA region, particularly Kuwait, remains a gray area. This episode of MENA MedTech Insights cuts through the ambiguity, offering a clear, experience-based perspective on how your MDSAP certification can impact your medical device registration in Kuwait. We move beyond official regulations to discuss the practical, on-the-ground reality. Learn how leveraging your existing

en

03:25

Qatar's MedTech Vigilance: A Pure Global Deep Dive...

MENA MedTech Insights ·

2025/08/29

In this episode of MENA MedTech Insights, we provide a crucial guide to the post-market surveillance (PMS) requirements for medical devices in Qatar. As one of the fastest-growing healthcare markets in the Gulf Cooperation Council (GCC), Qatar's regulatory environment, overseen by the Ministry of Public Health (MOPH), demands rigorous post-market vigilance from manufacturers to ensure patient safety and maintain market access.We move beyond theory to break down the essential components of a

en

03:16

Pure Global's MENA MedTech Insights: Why Your CE Mark...

MENA MedTech Insights ·

2025/08/28

In this episode of MENA MedTech Insights, we debunk the common myth that a CE mark is an all-access pass to the Middle East and North Africa's booming medical device market. While essential, it's only the first step. We explore the nuanced "CE-plus" regulatory models in key jurisdictions that often surprise even experienced manufacturers.We break down the specific requirements for market entry into powerhouse markets like Saudi Arabia and the United Arab Emirates. Learn why local representation,

en

03:01

Pure Global's MENA MedTech Insights: A Step-by-Step...

MENA MedTech Insights ·

2025/08/27

This episode of MENA MedTech Insights provides a detailed guide to registering a Class II medical device in Jordan. We explore the critical role of the Jordan Food and Drug Administration (JFDA) and break down the essential steps for foreign manufacturers, from appointing a local representative to compiling a compliant technical dossier.We delve into the specific documentation required, including the importance of prior approval from reference markets like the EU or USA. Learn about common

en

03:22

Beyond the Fees: Pure Global Reveals the True Cost of...

MENA MedTech Insights ·

2025/08/26

This episode of MENA MedTech Insights dives deep into the true cost of medical device registration in the GCC, moving beyond the well-known government fees. We uncover the various hidden expenses that can surprise manufacturers, including mandatory local representation, document translation, and embassy legalization costs, providing a realistic financial picture for entering key markets like Saudi Arabia and the UAE.Imagine a European stent manufacturer budgeting $4,000 for SFDA fees in Saudi

en

02:36

Pure Global Presents: Decoding Egypt's Arabic...

MENA MedTech Insights ·

2025/08/25

This episode of MENA MedTech Insights dives deep into a crucial, and often underestimated, aspect of entering the Egyptian medical device market: the strict Arabic labeling requirements set by the Egyptian Drug Authority (EDA). We explore the dual-language mandate and uncover the common pitfalls that can lead to significant delays and financial losses for manufacturers. Imagine your company has spent millions on product development and is ready to launch in Egypt, a key MENA market. Your shipment

en

03:10

Pure Global MENA MedTech Insights: Choosing Your...

MENA MedTech Insights ·

2025/08/24

In this episode of MENA MedTech Insights, we tackle a critical strategic decision for any medical device manufacturer looking to enter the Kingdom of Saudi Arabia: choosing your Authorized Representative (AR). This SFDA requirement is more than a formality; it's a choice that can define your operational freedom and long-term success in the market. We explore the two main pathways: appointing your distributor versus partnering with an independent, third-party AR. While naming your distributor seems

en

03:15

Pure Global's MENA MedTech Insights: Navigating SFDA...

MENA MedTech Insights ·

2025/08/23

This episode of MENA MedTech Insights dives deep into the complex world of medical device classification across the Middle East and North Africa. We move beyond the basics of risk-based classes to uncover the single most important factor for market access: reference country approvals. Learn how regulators in key markets like Saudi Arabia and the United Arab Emirates leverage prior approvals from the FDA, EU, and others to shape their registration pathways. We break down the specific requirements

en

03:27

Pure Global's Expert Guide to UAE Medical Device...

MENA MedTech Insights ·

2025/08/22

The UAE boasts one of the most advanced healthcare systems in the MENA region, but accessing this lucrative market requires a deep understanding of the Ministry of Health and Prevention (MOHAP) regulations. This episode provides a practical, step-by-step guide for MedTech manufacturers aiming for successful market entry, transforming complex regulatory hurdles into a clear path to approval. We break down the entire process, from the non-negotiable first step of appointing a local Authorized

en

03:01

Cracking the Code: A Pure Global Playbook for SFDA...

MENA MedTech Insights ·

2025/08/21

This episode of MENA MedTech Insights dives deep into the specific requirements for medical device registration with the Saudi Food and Drug Authority (SFDA). We uncover the critical steps and common pitfalls foreign manufacturers face when trying to enter one of the largest and fastest-growing healthcare markets in the Middle East. We explore why your choice of a local Authorized Representative can make or break your market entry strategy and how leveraging existing approvals from bodies like the

en

02:45

Cracking the Saudi Arabia MedTech Market: A Pure...

MENA MedTech Insights ·

2025/08/19

In this episode of MENA MedTech Insights, we demystify the process of medical device registration in Saudi Arabia. We explore why the Saudi Food and Drug Authority (SFDA) is a critical gatekeeper to one of the fastest-growing healthcare markets and break down the common hurdles that international manufacturers face.We move beyond the basics of GHTF prerequisites and dive into the specific nuances of the SFDA's requirements. Learn why your CE Mark or FDA clearance is only the beginning of the journey

en

91 results

Similar Podcasts

Classic Radio Science Fiction

solgoodmedia.com

Mission to Mars

Inception Point Ai

The 365 Days of Astronomy

365DaysOfAstronomy.org

Creek Devil

william Jevning

UFO Chronicles Podcast

Nik Hunter