Medical Device made Easy Podcast
Technology
A quality culture seem to be a nice to have. But after listening this podcast episode with Lesley Worthington, you will see that it is worth to build one. We will review the description of a quality culture and how to build it. But also if this is required by a regulation and how you can align it with your compliance duties. Check this and share it with your team.
Who is Lesley Worthington?Lesley works with individuals and teams to fine-tune their Quality conversations, initiatives, and internal communications to create a better understanding of the role and concepts of quality assurance throughout their organization.
Through her leadership and executive coaching, she supports professionals as they work on improving their relationships and effectiveness in their roles allowing them to achieve their fullest potential, professionally, and empowering them to move their organizations toward a robust Quality Culture.
She runs a community, The Quality Network, which supports Quality professionals as they work on the skills that allow them to build a Quality Culture. The Quality Network is a place for learning, coaching, support, and networking and includes webinars, resources, a member platform, courses, and office hours.
She combines 20 years of quality and regulatory experience in medical devices, in Canada, with thousands of hours of teaching and coaching to provide her clients with the skills, techniques, insights, and mindset that raise their confidence, take their communication skills to the next level, and allow them to have a positive impact in their organizations.
She’s got a Psychology Degree, a Law Degree, English as a Second Language Teaching Qualifications, and is a Certified Executive Coach.
Who is Monir El Azzouzi?Monir El Azzouzi, a distinguished expert in the medical device sector, holds a Biomedical Engineering degree from ISIFC in France. With extensive experience at top-tier companies such as Bausch+Lomb, Aesculap, and Johnson & Johnson, Monir has a deep understanding of the industry’s challenges and opportunities. His commitment to enhancing industry standards and support led him to establish Easy Medical Device.
Easy Medical Device is an innovative company dedicated to enriching the medical device community through educational outreach such as podcasting, blogging, and video creation. The company also offers specialized training programs, notably the Green Belt Certificate for EU MDR, to elevate professional skills within the industry.
Beyond education, Easy Medical Device provides comprehensive consulting services, helping manufacturers navigate the complexities of CE Marking, FDA registration, clinical evaluation reports, internal audits, design and development, supplier reviews, eQMS implementation, and due diligence. Our expertise extends to acting as authorized representatives and importers in Europe, Switzerland, and the UK, facilitating smoother market entry for our clients.
Monir’s vision for Easy Medical Device is to establish it as the definitive one-stop shop for all services related to medical device manufacturers. We are committed to assisting you in introducing and advancing your projects with efficiency and compliance.
Do not hesitate to contact Monir El Azzouzi at Easy Medical Device to explore how we can support your medical device initiatives.
LinksThe post Why and how to build a Quality Culture? appeared first on Medical Device made Easy Podcast. hamza benafqir
Why Design History File (DHF) is so important? [Alexandros Savvidis]
Medical Device News: February 2022 Regulatory Update
MDCG 2021-27 Placing on the market & Re-labelling with Erik Vollebregt
How to interview your QA RA Candidates? [Mitch Robbins]
How to accelerate your Laboratory Test Results? [Christoph Lindner]
Medical Device News – January 2022 [Happy New Year]
What happened in 2021? Summary for the Medical Device Industry
The Step-by-Step recipe to get MDR & IVDR Certified
Which devices cannot be Custom-made? [Erik Vollebregt]
Medical Device News: December 2021 Regulatory Update
Let’s unleash “MDR Classification surprises” [MDR 2017/745]
How to approach your Notified Bodies? [Dr. Royth von Hahn – TÜV SÜD]
Is it possible to Private Label a Medical Device under MDR & IVDR?
How to improve your QA RA Communication with Lesley Worthington?
Medical Device News – November 2021 latest update
How does the EU Commission plan to save IVDR 2017/746?
How to comply with MDR when products contain CMR Substances?
EUDAMED Update: Should you register your medical devices now?
Medical Device News – October 2021 Regulatory Update
Why does an Importer/Distributor need to appoint a Notified Body?
Create your
podcast in
minutes
It is Free
Insight Story: Tech Trends Unpacked
Zero-Shot
Fast Forward by Tomorrow Unlocked: Tech past, tech future
The Unbelivable Truth - Series 1 - 26 including specials and pilot
Lex Fridman Podcast