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www.huntingdon.com www.harlan.com Fiona McGuinness 29 April 2015 Harmonising Formulation Analysis Procedures
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www.huntingdon.com www.harlan.com Introduction What is best practice? Why harmonise? What will be harmonised? Harmonisation process Discussion
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www.huntingdon.com www.harlan.com Best Practice? 3 sites doing 3 separate procedures White paper? What parameters and acceptance criteria examined?
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www.huntingdon.com www.harlan.com Why Harmonise? One company, one process Opportunity to look at processes and make changes or improvements Discuss experiences to decide which way is the best way
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www.huntingdon.com www.harlan.com What will be harmonised? Parameters examined: Validation Sampling of diet formulations for stability assessment Homogeneity assessment Stability trial formulation size Standard and extract stability Pre-dose analysis Number of samples for routine analysis Genetic toxicology support
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www.huntingdon.com www.harlan.com Method Accuracy and Precision Site 1: 6 replicates of lowest and highest concentrations Site 2: 3 replicates at lowest, intermediate and highest concentrations Site 3: 2 replicates at lowest, intermediate and highest concentrations
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www.huntingdon.com www.harlan.com Harmonised Approach 5 replicates at each lowest and highest levels
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www.huntingdon.com www.harlan.com Diet Stability Trials Site 1 Samples taken immediately after preparation into bags and stored ambient and frozen for specified time-points Site 2 In drum, at ambient storage. Samples taken from drum at specified time-points Site 3 Sample taken in glass jar and stored at ambient for 21 days
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www.huntingdon.com www.harlan.com Proposed Change Samples from drum at each time-point Frozen sample taken on Day 0 and stored for 22 days (or more if time allows)
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www.huntingdon.com www.harlan.com Not yet… working towards Pre-dose analysis
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www.huntingdon.com www.harlan.com Standard and Extract Stability Site 1: Assessed, at least 4 days to allow re-analysis if necessary Site 2: Not routinely done Site 3: Not routinely done
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www.huntingdon.com www.harlan.com Other validation parameters ParameterSite 1Site 2Site 3 LOD/LOQEstimated 3x BN and 10x BN Not calculated SpecificityControl vehicle extracted and examined for peaks LinearityAt least 5 standards over a 10-fold range R 2 ≥0.999 Back-fits within 10% At least 5 standards no fixed range R 2 ≥0.999 Back-fits within 20% At least 5 standards no fixed range R 2 ≥no criteria Back-fits no criteria System Precision6 injections of lowest and highest standards CV≤2% 6 injections of mid- concentration standard CV≤2% Not routinely done
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www.huntingdon.com www.harlan.com How do you decide? Highlight similarities?
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www.huntingdon.com www.harlan.com Other validation parameters ParameterSite 1Site 2Site 3 LOD/LOQEstimated 3x BN and 10x BN Not calculated SpecificityControl vehicle extracted and examined for peaks LinearityAt least 5 standards over a 10-fold range R 2 ≥0.995 Back-fits within 10% At least 5 standards no fixed range R 2 ≥0.995 Back-fits within 20% At least 5 standards no fixed range R 2 ≥no criteria Back-fits no criteria System Precision6 injections of lowest and highest standards CV≤2% 6 injections of mid- concentration standard CV≤2% Not routinely done
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www.huntingdon.com www.harlan.com Calibration Standard Acceptance Over to you…..
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www.huntingdon.com www.harlan.com Any questions or further discussion points??
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