ZARZA We are Zarza, the prestigious firm behind major projects in information technology.

Medical Device made Easy Podcast

Medical Device made Easy Podcast

Por: Monir El Azzouzi

Listen Medical Device Regulation and Standards

89 episodios disponibles

Latest episodes of the podcast Medical Device made Easy Podcast

Prepare your transition from Class I to Class Ir 28/02/2023

SaMD international reach – What to consider? 21/02/2023

Biological Evaluation: Top Big mistakes 14/02/2023

Medical Device News: February 2023 Regulatory Update 06/02/2023

How to do Post-Marketing Surveillance in the US (vs EU)? 31/01/2023

How to evaluate Benefit-Risk Ratio for Medical Devices? 24/01/2023

Breaking News: EU MDR Extension Proposal is out for consultation 17/01/2023

How to improve the relationship between QA – RA and Marketing? 10/01/2023

Medical Device News: January 2023 Regulatory Update 03/01/2023

Grow your LinkedIn Profile with Karandeep Badwal 27/12/2022

Is EU MDR extended? with Erik Vollebregt 20/12/2022

MDCG, Team-NB, BVMed & Team-PRRC tell you all about PRRC 13/12/2022

Medical Device News – December 2022 Regulatory Update 06/12/2022

How to choose the best Sterilization Method for Medical Devices? 29/11/2022

Why Risk Management is important to Medical Device development? 22/11/2022

Regulatory Pathway: How to reach the US market? [510k exempt] 15/11/2022

Your Software/IVD clinical report is completely WRONG! 08/11/2022

Medical Device News – November 2022 Regulatory Update 01/11/2022

Can you go to Jail as a PRRC? [Elem Ayne] 25/10/2022

How to be MDSAP certified for your Medical Devices? 18/10/2022

1 2 3 ... 5 Siguiente › Última »