This FDA compliance training offers pragmatic approach to dealing with FDA mandated quality systems. The approach offered emphasizes function over form. Anyone subject to 21 CFR Parts 210, 211 and 820 will benefit from this seminar.
This course addresses questions such as 'how much documentation is enough?' and 'what is the appropriate level of rigor for my process validation?'
This course addresses questions such as 'how much documentation is enough?' and 'what is the appropriate level of rigor for my process validation?'
Areas Covered in the seminar:
- Simplifying GMP Documentation
- Strategies for Validation/Qualification
- Strategies for Effective Investigations
Who Will Benefit:
- QA Personnel
- Technical Writers
- Investigators
- Validation Engineers
- Manufacturing Operations Personnel
Course Provider
Garry Bandel,
