Medical Device made Easy Podcast

Design History File (DHF) remediation is rarely planned — yet it is a recurring challenge for many medical device manufacturers, especially during audits, inspections, acquisitions, or regulatory fram...

22 Jan 0s

Social Media to follow The post Medical Device News January 2026 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir

15 Jan 0s

Verification & Validation (V&V) plays a central role in ensuring that medical devices are safe, effective, and compliant — yet it remains one of the most challenging phases for many […] The post Verif...

7 Jan 0s

As the year closes, this special podcast episode offers a comprehensive overview of what happened at Easy Medical Device in 2025 and the key priorities shaping 2026. The episode reflects […] The post ...

31 Des 20250s

The European medical device sector is a vital pillar of healthcare innovation, employing over 930,000 people and representing a market of approximately €170 billion. However, since the implementation ...

24 Des 20250s

Clinical Evaluation has become one of the most critical — and challenging — domains under the EU MDR. But how does one build real expertise in this field? In this […] The post From Engineer to Clinica...

17 Des 20250s

Medboard Europe UK Standard EasyIFU Rest of the World Argentina Canada Brazil: Podcast Podcast Nostalgia – Let’s review previous podcasts Social Media to follow The post Medical Device News DECEMBER 2...

11 Des 20250s

Becoming a Lead Auditor is one of the most valuable career steps for quality and regulatory professionals in the MedTech sector. Lead Auditors play a critical role in evaluating QMS […] The post How t...

4 Des 20250s