Developing an Effective CAPA Program for GMP Operations 2015
12 Oct 2015
Online Event
Description
Topics
Roles and responsibilities of manufacturers
Hy an effective CAPA system is important
Determining root causes
Identifying sources of infractions
CAPA Tracking System and documentation
Who should Attend
Quality Assurance scientists
Laboratory Analysts
QA/QC Managers
QA/QC Analysts
Inspectors
Auditors
Manufacturers of raw materials and excipients
Pharmaceutical development and manufacturing personnel
Contract laboratory Organization personnel
Past Events
Developing an Effective CAPA Program for GMP Operations 2015 - 12 Oct 2015, Online Event (54214)
Important
Please, check "Developing an Effective CAPA Program for GMP Operations" official website for possible changes, before making any traveling arrangements
