Siemens Nederland N.V FDA13April Presented by Troy Logan at the Advisory Committee for Pharmaceutical Science meeting on April 13, 2004
Siemens Nederland N.V FDA13April for internal use only Siemens – PAT solution in pharmaceutical industry
Siemens Nederland N.V FDA13April Reducing production cycle times Right first time quality (RFT) Preventing rejects, scrap, re-processing Managing variability (improving energy and material use and increasing capacity) Facilitating continuous processing (improve efficiency) Increasing automation to improve operator safety and reduce human errors Real time release PAT opportunities (FDA’s PAT Draft Guidance)
Siemens Nederland N.V FDA13April Ultimate step – Real Time Product Release Production and release of pharmaceuticals, without final tests Quality is based only on review of process characteristics
Siemens Nederland N.V FDA13April Standardized over the complete unit BioreactorHarvest & separation PurificationBuffer + Medium FormulationFinishingPackaging
Siemens Nederland N.V FDA13April Multidisciplinary approach Process Analytics Chemometrics / MVDA Process under- standing (advanced) Controls Process development Modelling MES regulatory
Siemens Nederland N.V FDA13April PROCESS Control Process Monitoring PAT concept IT / MES INFRASTRUCTURE Process Analytics process Specif. verification real-time product release monitoring iterative learning control (process) knowledge optimization control modules electronic batch record equipment modules pharma modules batch
Siemens Nederland N.V FDA13April Real Time Product Release Process output Temperature, pH, pO2 pressure Close loop control (physical / chemical parameters only) parameters only) Process feed Off lineOn line Required Process information PAT Iterative Learning Control QualitativeQuantitativeFingerprint Transform to quality data Product M Bio- reactor Monitoring Temperature, pH, pO2, pressure Lab based review of product quality holdrelease
Siemens Nederland N.V FDA13April Infection detection with PAT B. subtilis, C. albicans, S. aureus, E. coli, Ps. Aeruginosa, A. niger and L. Brevis Infected (10 2 CFU / ml )Non infected on yeast based fermentation and substrate samples: Biological contamination
Siemens Nederland N.V FDA13April Bioreactor process monitoring In-situ NIR Probe
Siemens Nederland N.V FDA13April Use of PAT as qualitative tool Example vaccine production Process track monitoring and early detection of disturbances Scores plot for the two main principal components on collected spectra during the batch process Process pattern : process fingerprint / signature (multidimensional profile) Comparing “fingerprints” of different batches Change in process status Disturbance Start End
Siemens Nederland N.V FDA13April Process Path definition Data analysis PAT implementation Road Map Product Q assessment Process assessment analyzer assessement Risk assessment 1. Measure (Monitoring + Process understanding) Process control definition (ideal process runs) Process control for process corrections Knowledge + Change management Continuous optimization & improvement 2. Control 3. Optimization Time Validation Plan People & organizatio- nal Managm.