medical device academy

0:06:51

What does Medical Device Academy do?

0:01:26

Medical Device Academy's 510(k) Course and Webinar Series

0:03:45

What makes Medical Device Academy different?

0:11:50

What is the best way to perform risk management?

0:14:42

What is the best approach to private labeling medical devices?

0:11:12

What is ISO 13485?

1:24:32

Six steps to ISO 13485:2016 Certification and MDSAP Certification

0:12:06

What is a Class 1 and 2 device exemption?

0:27:26

How do clinical trials work for a medical device in the USA?

0:19:05

How review medical device labeling

0:19:31

Rob Packard - Founder and President of Medical Device Academy Inc.

0:16:10

Which topics should you prioritize for an FDA pre-sub meeting?

0:02:10

What Does Medical Device Academy Do?

0:20:46

What's the difference between the process approach to auditing? using an audit checklist? and QSIT?

0:03:02

What's new this week at Medical Device Academy?

0:02:23

What is and is not included in Medical Device Academy's flat fee pricing?

0:27:58

Software Validation for Medical Devices – FAQs

0:17:20

What is a preamendment device?

0:00:36

Rob Packard – Medical Device Academy – 10x

0:02:29

Medical Device Academy at Medica in Dusseldorf, Germany

0:06:50

Who Is Medical Device Academy

0:02:45

FDA eCopy services- Medical Device Academy

0:18:53

What is the regulatory pathway for a De Novo medical device or IVD?