PRISYM ID will host a Webinar on ‘The Compliance Crackdown: Guarding Against FDA Action’ at 8:00 am. PT / 11:00 am. ET / 4:00 pm. GMT on Tuesday, February 7th, 2012. The webinar will explore what is required for compliance and how to achieve it.
The FDA is cracking down when it comes to FDA 21 CFR Part 11 compliance. The last few years have shown an increase in the number of inspections, seizures, injunctions, Warning Letters, and recall events; and penalties are being enforced to discourage future offenses. In addition, companies need to be faster than ever to respond to any action taken by the FDA. Less leniency is being given for the 15-day period to respond to an FDA Warning Letter and an FDA injunction can now be issued prior to even sending a Warning Letter.
Benefits of attending:
- Learn what it means to be FDA 21 CFR Part 11 compliant
- Gain awareness of the most common compliance pitfalls and how to avoid them
- Discover how software can aid your business when designing, producing and managing labels
- Understand how costs can be significantly reduced while gaining and maintaining strict compliance global regulations and standards
In this 60-minute, information-packed session, experts from PRISYM ID will present an in-depth look at what is required for compliance and how to achieve it to avoid action being taken by the FDA. It will also discuss tips on how to ensure your label design, approval, management and production processes are secure.
About PRISYM ID Limited
PRISYM ID (prisymid.com) design and deliver high quality labeling and identification solutions for organizations that need complete product auto-identification and lifecycle traceability. Headquartered in the UK, with offices in Europe and the US, the company supplies a comprehensive range of software and consumables for a wide range of sectors to an elite customer-base.