Copyright © 2010 All rights reserved Freije Quality Engineering, LLC

Veteran Owned Business

We recognize the need to stay abreast of the ever changing regulated environment.
 We are consistently updating our knowledge with the FDA’s current thinking by reviewing the latest industry regulations, guidance documents, warning letters, and attending outside training to stay current with Good Manufacturing Practices (cGMP).
Not only do we review the latest industry trends, but we also spread our leadership knowledge in the compliance industry by authoring published articles, providing feedback to guidance documents, participating in development/peer review of industry course curriculums, and facilitating industry discussion group meetings.

Why Freije Quality Engineering?

When you operate in a highly regulated industry, such as manufacturing of medical devices, your goal is to operate in a continual state of compliance.

 

Freije Quality Engineering provides cost effective FDA and ISO Quality Systems compliance consulting that helps you achieve this state of continual compliance without overburdening your company’s operations.