Description

There is no question that medical device manufacturing is a complex and highly regulated industry. So how do you make the regulatory burdens work to your organization’s benefit? Join Stefan Koch, from Frontwell Solutions, Jeff Richardson, from Critical Manufacturing and Rogério Ferreira from Critical Manufacturing for a lively and interactive discussion about the role an MES plays in medical device manufacturing. The discussion will focus on reducing paper, maintaining compliance, and automating your validation using reasonable, efficient, and modern methodologies. The table is packed with other essential topics as well including what an MES will mean for quality, costs, and risk in 2023.

Register here.