One of the
greatest challenges facing the medical device industry is regulatory
compliance. In a rapidly changing
environment, organizations must adhere to the requirements and standards set
forth today, and constantly anticipate the changes of tomorrow.
There is an
immediate need to build robust processes and systems to ensure regulatory
obligations and reporting requirements are being met. The principal objective of ISO 13485 is to
facilitate harmonized medical device regulatory requirements for quality
management systems.
Attend this
webinar to learn the following:
We invite
you to attend this webinar whether you are in manufacturing, regulatory
affairs, product design, research and development, quality assurance and
control, management of medical device operations, or medical marketing
personnel.
About the Presenter
John
Cachat is an expert in developing information technology and operational
excellence strategies for large and small organizations. Mr. Cachat is
often sought out for his expertise by large consulting firms, like IBM
Consulting, government agencies, like the US FDA, and professional and trade
organizations for his leadership.
Mr. Cachat received a BSIE degree at the General Motors Institute (GMI) in
Flint, MI specializing in Operations Research, and received recognition for
both the Entrepreneur of the Year and Outstanding Alumni Achievement awards
from GMI. John also holds an MSIE degree from Texas A & M
University, specializing in automated manufacturing.