Maximising HPLC Productivity
18 - 20 April 2012
Conference
Prague, Czech Republic
The purpose of this course is to provide attendees with practical information to manage HPLC within GMP-/FDA-regulated environments of the pharmaceutical industry by combining science and compliance. The emphasis will be on the following science and compliance issues:
- Miniaturisation of HPLC: advantages and disadvantages
- Sampling practices and pitfalls
- Sample preparation for HPLC
- Latest enforcement issues and lessons for CDS
- Science driven HPLC qualification
- Method development and validation including understanding and trouble shooting problems
- USP and EP system suitability tests
- Practical chromatographic integration
- Better working to avoid OOS investigations
- Generating productivity gains through the validation of a CDS
- Defining and protecting CDS electronic records
- Documentation for HPLC
Organiser: Concept Heidelberg