Expert Talk: Optimizing Compliance in the Pharmaceutical Industry
Register for this live expert talk – and find out how to optimize your GMP/GAMP pharma compliance process! Make it simpler and yet more comprehensive!
Two top pharma experts – Georg Roth, head of Anton Paar’s pharma qualification services, and Yves Samson, founder of Keron AG, an e-compliance consultancy firm in Basel, Switzerland – will discuss the holistic approach to compliance, which comprises patient safety, product quality, and data integrity. You’ll get to ask them questions afterwards in a live Q&A session.
Remember: Anton Paar has 80+ solutions for speeding up your pharma instrument qualification and requalification!
- QI: Detailed instructions for all qualification steps and test points
- DQ: As-built specification and risk analysis
- IQ: Detailed individual test points for complete installation and all relevant certificates (e.g., for wetted parts, software certificates, etc.)
- OQ: Detailed protocols of measured reference values with limits, protocols of performed checks and eventual adjustments, and 21 CFR Part 11 checklist
- PQ: Detailed report of customer samples
- FQ: Deviation list and traceability matrix leading to a final qualification report
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