fme compliance-center™ is the premier platform for executing your validation requirements while leveraging the efficiency of the newest CSA methodology. Based on the CSA guidelines and our 25 years of working with global pharmaceutical, medical, and other industries with strict compliance requirements, fme compliance-center is specifically built to streamline validation workflows with an efficient risk-based methodology.
This solution can help reduce overall costs and bring your product to market quicker and with higher quality. The team at fme can expertly validate any solution for you and can provide fme compliance-center™ as a QMS to use for your own projects.
- Regulatory Information Managers
- Qualty and Manufacturing Managers
- IT Managers
- Life Sciences
- Additional Industries
- Increased Quality – Focusing efforts on high-risk processes allows for a better overall system quality
- Decreased Risk – Following the updated guidelines provided by the health authority reduces the risk of issues
- Less Documentation – More time is spent on critical thinking, and less time editing, reviewing, and printing documents
- Lower Costs – Less time spent on tedious tasks translates to a more efficient and cost-effective process that saves time and money
- Faster Implementation – A more efficient process also means a quicker review, approval, and go-live date
Don't like forms? Contact us directly to get more details on any of fme's services. We'd love to discuss your current challenges, and how fme can help you get the highest ROI and lowest TCO for your technology solutions. Call or use my personal contact form with your question, and I'll get you connected with the right fme expert.
fme is always looking for top talent to join our team. If you are looking to join the team you'll love to work with, review our job listings and review the details of current openings. Contact me if you have any questions on the application process.