Batch Production Record and Device History Record Review and Quality Assessment 2014
13 Aug 2014
Webinar
Key Topics
Production and In-Process Controls
Generation of BPRs, DHRs and SOPs to provide technically written instruction sets to eliminate operator errors. Training is NOT the primary means of generating and error free operation
Responsibilities for Production Activities
Inspection, Packaging and Identification Labeling of Finished Products and Intermediates
Incident / Deviation Tracking along with Customer Complaints and CAPA changes
Data selection and entry into the statistical tracking from the BPR and DHR
Annual Reports
Who should Attend
Documentation Personnel
Quality
Past Events
Batch Production Record and Device History Record Review and Quality Assessment 2014 - 13 Aug 2014, Webinar (37622)
Batch Production Record and Device History Record Review and Quality Assessment 2026
Important
Please, check "Batch Production Record and Device History Record Review and Quality Assessment" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical technology, Pharma
