Medical Device made Easy Podcast
easymedicaldevice
My name is Monir El Azzouzi and I am a Medical Device Expert specialized in Quality and Regulatory affairs. And on this podcast I will help you place compliant medical devices on the market. For that I will share with you my knowledge or the one of others through discussion or interviews. I will invite experts in the area to tell you what you can do or the challenges you may encounter.
Kategorier: Näringsliv
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308 - Radiation Sterilisation Master File (ISO 11137 & 11607)Tue, 09 Apr 2024
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307 - Medical Device News April 2024 Regulatory UpdateThu, 04 Apr 2024
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306 - ow to benefit from Surveys to build Clinical Evidence?Tue, 26 Mar 2024
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305 - How to do Postmarketing Surveillance the right way?Tue, 19 Mar 2024
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304 - FDA aligns QMSR with ISO 13485?Tue, 12 Mar 2024
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303 - Medical Device News March 2024 Regulatory UpdateWed, 06 Mar 2024
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302 - New EU Proposal - EUDAMED, IVDR & ShortageTue, 27 Feb 2024
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301 - Will EtO gaz become a Medical Device?Tue, 20 Feb 2024
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300 - How to get your interview prepared?Tue, 13 Feb 2024
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299 - Medical Device News february 2024 Regulatory UpdateWed, 07 Feb 2024
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298 - Why you should use Pre-Submission or Q-Sub with FDA?Tue, 30 Jan 2024
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297 - You are not the Physical Manufacturer, can you be MDR certified?Tue, 23 Jan 2024
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296 - MEDICA 2023 - InterviewS with Startups, Service Providers, Notified Bodies...Thu, 18 Jan 2024
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295 - WARNING! APPLY TO YOUR NOTIFIED BODY NOW!Tue, 16 Jan 2024
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294 - Medical Device News – january 2024 Regulatory UpdateWed, 10 Jan 2024
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293 - Regulatory Maturity Model – Heatmap (MEDICA 2023)Tue, 02 Jan 2024
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292 - Life of QA RA Podcasters?Tue, 26 Dec 2023
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291 - Why should you invest in your Regulatory Team?Mon, 18 Dec 2023
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290 - What is Usability for Medical Devices?Tue, 12 Dec 2023
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289 - Medical Device News: December 2023 Regulatory UpdateWed, 06 Dec 2023
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288 - What is the situation regarding digitalization in Medtech?Tue, 28 Nov 2023
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287 - How to find your Predicate Device for your 510K Submission?Tue, 21 Nov 2023
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286 - How to CE certify a Calculator, Risk Score…?Tue, 14 Nov 2023
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285 - Medical Device News – November 2023 Regulatory UpdateThu, 09 Nov 2023
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284 - Validate your Iphone, Samsung Galaxy, Huawei… for your SoftwareTue, 31 Oct 2023
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283 - Afrisummit 2023 Interviews Part 2 – Egypt SituationTue, 24 Oct 2023
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282 - Afrisummit 2023 Interviews Part 1Tue, 17 Oct 2023
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281 - What are some pitfalls to avoid during Software Design?Tue, 10 Oct 2023
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280 - MEDICAL DEVICE NEWS October 2023 Regulatory UpdateWed, 04 Oct 2023
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279 - What is the EUDAMED Update?Tue, 26 Sep 2023
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278 - Interviews on Being The PRRCTue, 19 Sep 2023
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277 - Interviews on Being The PRRCWed, 13 Sep 2023
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276 - MEDICAL DEVICE NEWS – SEPTEMBER 2023 Regulatory UpdateWed, 06 Sep 2023
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275 - How to perform your Cleaning Validation in practice?Tue, 29 Aug 2023
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274 - What are the Acceptance Criteria for your Clinical Evaluation?Tue, 22 Aug 2023
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273 - Why you should automate your Software validation?Tue, 15 Aug 2023
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272 - Hire your QA RA person with no BudgetTue, 08 Aug 2023
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271 - Who should be on your Risk Management Dream Team?Tue, 01 Aug 2023
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270 - Artificial Intelligence in the Medical Device IndustryTue, 25 Jul 2023
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269 - Validation of Quality Softwares in MedDevTue, 18 Jul 2023
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268 - How to register Medical Devices in Saudi ArabiaTue, 11 Jul 2023
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267 - Medical Device News - July 2023 Regulatory UpdateTue, 04 Jul 2023
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266 - What should you know on UKCA extensionTue, 27 Jun 2023
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265 - How to connect Software dev and QA RA TeamTue, 20 Jun 2023
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264 - The great misunderstanding of EU MDR amendmentsTue, 13 Jun 2023
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263 - Medical Device News -June 2023 regulatory updateThu, 08 Jun 2023
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262 - How to master regulatory intelligenceTue, 30 May 2023
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261 - What if your Medical Device company goes Bankrupt?Tue, 23 May 2023
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260 - Technical Files Inconsistencies identified by Notified BodiesTue, 16 May 2023
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259 - The truth about the UK vs EU situationTue, 09 May 2023
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