The 2011 webinar in May will cover the following topics:
- Costs of system retirement
- Documentation of the retirement process
- Planning and conducting system retirement
- Responsibilities for system retirement
- Criteria for reprocessing of data
- Risk based archiving of e-records
- Strategies for data migration and retrieval
- FDA and Part 11
- FDA and international regulations
The event brings together CROs, Contract laboratories, Medical device industry, Pharmaceutical development and manufacturing, Pharmaceutical Research, Consultants, Training departments, Regulatory affairs, QA/QC managers and personnel, GLP/GMP auditors, Operation managers, supervisors and staff, IT Managers and staff.
