FDA Regulations for Analytical Instrument Qualification and Validation Processes 2017 is a webinar that covers topics such as:
- Risk based validation approach
- Requirements and approaches for Analytical Instrument Qualification
- User requirements, writing the specifications
- Going through the qualification phases
- Proper documentation
- Testing and deviation handling
- Periodic review and revalidation analytical instruments and equipment
- Type and extend of qualification for USP Instrument Categories
- Wrap up - Final questions and answers
FDA Regulations for Analytical Instrument Qualification and Validation Processes 2017 is intended for:
- IT managers and staff
- Laboratory managers, supervisors and analysts
- Laboratory suppliers of material, equipment and services
- Consultants
- Quality professionals
- Senior quality managers
- Compliance professionals
- Regulatory professionals
- Validation engineers
- Production supervisors
- Production engineers
- Manufacturing engineers
- Process owners
- Design engineers
- Quality auditors
- Quality engineers
