7 Podcast Episodes
051 - "EU MDR" with Bassil Akra
051 - "EU MDR" with Bassil Akra
On this episode, I was joined by Bassil Akra, the CEO of AKRA Team. Bassil and I discuss: EU MDR and Implementation Tim... Read more
21 Sep 2022
•
44mins
Traversing the Medtech Regulatory Landscape in the Interest of Patients with Dr. Bassil Akra, CEO of AKRA TEAM GmbH
Traversing the Medtech Regulatory Landscape in the Interest of Patients with Dr. Bassil Akra, CEO of AKRA TEAM GmbH
Dr. Bassil Akra, CEO of AKRA TEAM GmbH, takes a deep dive into the new approval process for medical devices in the EU an... Read more
6 Jul 2022
•
31mins
How to interpret the first Expert Panel Opinion? [Bassil Akra]
How to interpret the first Expert Panel Opinion? [Bassil Akra]
We received the First Expert Panel Opinion and by reading it you can say a lot. So to help us have a good interpretation... Read more
13 Jul 2021
•
Do you need an Expert Panel for your Medical Devices? [Bassil Akra]
Do you need an Expert Panel for your Medical Devices? [Bassil Akra]
The EU MDR 2017/745 is increasing the requirements for Clinical Evaluations. In this episode, I will be with Dr. Bassil ... Read more
16 Nov 2020
•
What means Sufficient Clinical Data with Bassil Akra (EU MDR)
What means Sufficient Clinical Data with Bassil Akra (EU MDR)
You are maybe trying to build your Clinical Evaluation Report or your PMCF for a Medical Device. And you are stuck becau... Read more
1 Jun 2020
•
What is the Notified Body situation? (Bassil Akra from TUV SUD)
What is the Notified Body situation? (Bassil Akra from TUV SUD)
You are looking for a Notified Body for your Medical Device in the EU market but you don’t understand why this is so dif... Read more
25 May 2020
•
The Qmed Podcast #5 with Dr. Bassil Akra
The Qmed Podcast #5 with Dr. Bassil Akra
In this episode we're proud to welcome Dr. Bassil Akra. We are discussing the MDR - the new regulation and changes to co... Read more
10 May 2019
•
48mins