News by Tag: Us Seminar
2-day In-person Seminar on Effective Complaint Handling, Medical Device Reporting and Recalls
March 25, 2013
This seminar will familiarize participants with ways of putting an effective complaint handling system in place. A good complaint handling system is a sine qua non for any quality system.
March 25, 2013
This seminar will familiarize participants with ways of putting an effective complaint handling system in place. A good complaint handling system is a sine qua non for any quality system.
2-day In-person Seminar on Software Validation for the New FDA Inspections
March 25, 2013
Computer systems need to be compliant in relation to a few important areas. Some areas of regulation relating to implementation of computerized systems can be worked out for better results.
March 25, 2013
Computer systems need to be compliant in relation to a few important areas. Some areas of regulation relating to implementation of computerized systems can be worked out for better results.
Design of Experiments and Statistical Process Control for Process Development and Validation From GlobalCompliancePanel
January 4, 2013
The soul of this this course is a presentation of the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes.
January 4, 2013
The soul of this this course is a presentation of the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes.
Verification vs. Validation - Product, Process, Software and QMS From GlobalCompliancePanel
January 4, 2013
The FDA has new and tougher regulatory requirements for a company's Master Validation Plan for major key inputs and CGMP deficiencies.
January 4, 2013
The FDA has new and tougher regulatory requirements for a company's Master Validation Plan for major key inputs and CGMP deficiencies.