Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel 2012
24 Jul 2012
Webinar
Key Topics
Audit preparation
Examine key elements of an API audit
Audit itself
Opening Session
Discussion of findings
What to look for?
Closing Meeting
Suggestions and experience
Who should attend openning and closing sessions
Who should participate in audit
Follow-up Actions
Audit Reports
Follow-up Audits
Agreed upon Schedules
Who should Attend
Supervisors and Managers in Quality
Supervisors and Managers in Manufacturing
Maintenance Supervisors and Managers
Engineering
Warehousing and Materials Management Supervisors and Managers
Past Events
Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel 2012 - 24 Jul 2012, Webinar (31100)
Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel 2011 - 18 May 2011, Webinar (15822)
Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel 2026
Important
Please, check "Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Education: Training
Health & Medicine: Healthcare, Medical device, Pharma
