EMMA International offers webinars and quality management trainings on issues and solutions that are current in the medical device, pharmaceutical, and biotech industries including strategic insights on FDA regulations, compliance, strategy, products and scientific support.
In this webinar hosted from EMMA International's Lead Quality Engineer, Nikita Angane, she will go over the different FDA Centers, as well a...
In this webinar, we will be covering what exactly an SaMDs, or Software as a Medical Device, and go over some examples with Artificial Intel...
In this second part of the webinar, we will review how to tackle changes that were made to the software post market, the verification and va...
This webinar will explore the Medical Device Single Audit Program, or MDSAP. We will provide an overview of the program, including how the a...
Are you a manufacturer and want to help with the COVID-19 Pandemic? We invite you to attend our upcoming webinar to learn more about FDA’s...
Our Lead Quality Engineer, Nikita Angane, explains how to build a strong Quality Management System for your Software as a Medical Device....
Our Quality Engineer, Madison Wheeler, discusses the characteristics of an efficient product development process for medical devices and how...
Our Sr. Quality Engineer Matt Ward explains how to build a strong Design History File for your product by incorporating human factors engine...
Our RA Manager Song Seto guides you through the FDAs pathway to get your combination product to the US market. Learn more about the combo pr...
EMMA’s EMEA Regional Director Joseph Yammine explains how the EU’s General Data Protection Regulation applies to the Health Care Industr...