Mastering Internal Audits: Best Practices for Medical Device Companies

Mastering Internal Audits

Webinar Title:

Mastering Internal Audits: Best Practices for Medical Device Companies

Date: Tuesday, July 02, 2024

Time : 16.00 GMT / 11.00 EST

Description:

Join us for an insightful webinar where we will delve into the critical aspects of mastering internal audits for medical device companies. This webinar is designed to equip professionals in the medical device industry with the essential knowledge and practical steps necessary to conduct effective internal audits, ensuring compliance with regulatory requirements and enhancing overall quality management.

What You Will Learn:

  • Understand the key elements and importance of internal audits in the medical device industry.
  • Learn best practices for planning, conducting, and reporting internal audits.
    Gain insights into identifying and addressing non-conformities during internal audits.
  • Explore strategies for continuous improvement through effective audit processes.

Who Should Attend:

  • Professionals involved in quality assurance, regulatory affairs, and compliance within the medical device industry.
  • Manufacturers, engineers, and executives responsible for product development and manufacturing processes.
  • Anyone seeking a comprehensive understanding of internal audit practices and their implications for medical device companies.
  • Don’t miss this opportunity to enhance your knowledge and strategies for conducting effective internal audits. Register now to secure your spot!

Meet our Speaker: Dr. Fiona Masterson, The Learning Reservoir

Note: By registering for this webinar, you agree that your supplied contact information can be shared with the event presenter for the purpose of contacting you regarding this webinar and related information/products discussed within. The event host, Learning Reservoir, may also contact you regarding future webinars, events, newsletters, and related marketing materials. Please review our Privacy Policy for more information.

Fiona Masterson headshot Dr. Fiona Masterson brings extensive expertise in quality assurance and regulatory compliance within the medical device industry. With a background as a lead quality auditor and a seasoned professional in internal audits, Fiona has guided numerous medical device companies in achieving excellence through effective audit strategies. Her experience includes leading FDA audit-facing internal audit teams, ensuring alignment with regulatory requirements such as ISO 13485 and 21 CFR Part 820. 

For any inquiries, please contact info@thelearningreservoir.com

Webinar Host:

The Learning Reservoir

Explore our eLearning Hub: Enhance Your Medical Device Knowledge Further!

Discover our comprehensive suite of medical device eLearning courses in our eLearning hub. Dive deeper into various aspects of medical device regulations and best practices to elevate your expertise and ensure compliance.

Why Enroll?

  • Gain expert insights and practical knowledge.
  • Enhance your ability to manage and resolve quality issues.
  • Improve compliance with FDA regulations.

Don’t miss this opportunity to expand your skills and knowledge in medical device practices. Click the link below to explore our eLearning hub today!

Can we help you?

At The Learning Reservoir, we’re dedicated to supporting professionals in the medical device industry with their training and educational needs. Whether you’re looking to enhance your team’s skills with customized training programs, need assistance with regulatory compliance, or have any questions about our services, we’re here to help.

Contact us today to learn more about how we can tailor our services to meet your specific needs and help you achieve your goals in the medical device sector.

Explore our YouTube Channel

Did you know we have a wealth of educational content available on our YouTube channel? Our channel is your go-to resource for valuable content on topics related to the medical device industry.

Subscribe to our channel today to stay up-to-date with the  best practices, and expert advice in medical device manufacturing and quality management. Don’t miss out on this opportunity to expand your knowledge and take your skills to the next level!