Keeping up with regulatory change can expedite product approval, help you be better prepared for audits, and help inform business decisions.
Bedford, Massachusetts (PRWEB) September 24, 2014
Cognition Corporation, a provider of next generation product development and compliance software, announced today that it will host a series of live webinars to discuss the changing FDA regulations.
The first in the series will take place Wednesday, October 1, from 3:00PM to 4:00PM Eastern Daylight Time. This webinar will offer expert information from Michelle Lott, RAC. Michelle is Cognition’s Executive Regulatory Expert. Ms. Lott will give a recap of key initiatives released by the FDA over the summer of 2014.
“The regulatory environment is dynamic and changes can have far reaching impacts on design projects, product approvals, and business strategy,” explains Ms. Lott. “Keeping up with regulatory change can expedite product approval, help you be better prepared for audits, and help inform business decisions. In this webinar, we will review some of the more significant recent regulatory changes so you will be better equipped to successfully navigate this changing environment.”
The content discussed in the live webinar is directly related to the montly Pulse Checks Ms. Lott performs as part of her duties as regulatory expert. Registration for this live event can be completed at https://www1.gotomeeting.com/register/418536608. The event will be recorded for on-demand viewing at http://www.cognition.us.
Cognition Corporation, based in Bedford, Massachusetts, has been offering solutions for product and process development for more than ten years. Cognition offers two core products: Cognition Cockpit™ and Enterprise Cost Management™ (ECM). Thousands of users worldwide use Cockpit and ECM to manage their product development and to meet performance, cost, risk, and schedule targets. For more information, visit http://www.cognition.us or call +1 (781) 271-9300.