Complying With Gmp And C Gmp Requirements Streamlining Quality Assurance & Fda Compliance February 26, 2008

As part of Global Compliance Series of seminars, ComplianceOnline brings you the expert view on “Complying with GMP and cGMP Requirements – Streamlining Quality Assurance & FDA Compliance” by Jeff Kasoff, RAC, is the Director of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields.

This seminar will provide valuable assistance to all personnel involved in development, implementation, and maintenance of a quality system which is in compliance with FDA Good Manufacturing Practices. Top management will benefit from being aware of these requirements that their company must comply with. Regulatory and Quality Management will benefit from knowing what practices their personnel must comply with. Research and Engineering personnel will benefit from awareness of required research and development practices.