Reducing Drug and Device Batch Release Times: Improving your BPR/DHR Review and Assessment 2016 is a webinar that covers topics such as:
- Production and in-process controls
- Generation of BPRs, DHRs and SOPs to provide technically written instruction sets to eliminate operator errors
- 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
Reducing Drug and Device Batch Release Times: Improving your BPR/DHR Review and Assessment 2016 is intended for:
- Compliance personnel
- QA/QC personnel
- Process validation and Lean Six Sigma experts
- Manufacturing and operations executives
- SOP development and training executives
- Regulatory affairs professionals
