Laboratory Inspection Readiness - Implementing GMPS for the Pharmaceutical Laboratory 2017 is a webinar that covers topics such as:
- Personnel organization and records
- Types of inspections
- Key SOPs every lab should have, and related training and maintenance
- Instrument inventory, qualification and change control
- Documentation of analytical procedures, including validation, verification and change control
- Log of out of specification results
- Trending of analytical data, laboratory incidents and OOS reports
- Documentation of analytical data and reports
- Attendee questions and answers
- Brief introduction to expectations for computer systems
Laboratory Inspection Readiness - Implementing GMPS for the Pharmaceutical Laboratory 2017 is intended for:
- Laboratory Managers
- Chemists
- Quality Assurance personnel responsible for generating GMP or GLP data or assuring readiness for a regulatory inspection
- Regulatory Affairs
- Documentation
- IT/IS
