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.
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...
The purpose of this webinar is to discuss the FDA’s voluntary medical device manufacturing and product quality pilot program, CMMI Institu...
Presented by MichBio Member Company, EMMA International Consulting Group, Inc. EMMA International Consulting Group CEO, Dr. Carmine Jabri, ...
The ongoing changes in the international regulatory landscape will have a direct impact on quality management systems’ (QMS) design and im...
Having the ability to meet the customers’ requirements, comply with international standards and regulations, and mitigate potential risks ...
What You Need To Know About The New European Union Medical Device Regulation occurs several times. Please register for the date and time tha...