Dr. Ganapathy Subramanian is a biotechnology consultant with over 30 years of experience in industry and academia, encompassing the application and development of processing, purification methodologies, and chromatographic systems for large scale use in environmental science, food science, perfumery, cosmetics, and pharmaceuticals. He has also taught extensively in the area of food and medical technology. A chemistry graduate from Madras, India, Dr. Subramanian was awarded his doctorate from the University of Glasgow for work on natural products. His main research interests lie in the utilization of natural material separation processes and bioconversions. Dr. Subramanian has written and edited a number of books and articles in the field of biotechnology. For the last 15 years, he has been organizing conferences promoting the integration and sharing of knowledge between academia and industry.

• 1. Continuous Bioprocess Development: Methods for Control and Characterization of the Biological System2. Tools Enabling Continuous and Integrated Upstream and Downstream Processes in the Manufacturing of Biologicals 3. Engineering Challenges of Continuous Biomanufacturing Processes (CBP) 4. Progress Towards Automated Single Use Continuous Monoclonal Antibody Manufacturing via the Protein Refinery Operations Lab 5. Single-use bioreactors for continuous bioprocessing: challenges and outlook6. Two mutually enabling trends: Continuous bioprocessing and Single-use technologies 7. Perfusion Formats and their specific medium requirements 8. Upstream Continuous Process Development9. Study of Cells in the Steady State Growth Space 10. Continuous Downstream Processing for Production of Biotech Therapeutics11. Evolving Needs For Viral Safety Strategies in Continuous Monoclonal Antibody Bioproduction 12. Multi-Column Continuous Chromatography ? Understanding this enabling Technology13. Continuous Chromatography as a fully integrated process in Continuous Biomanufacturing14. Continuous Chromatography in Biomanufacturing 15. Single Pass Tangential Flow Filtration (SPTFF) in Continuous Biomanufacturing 16. Design of Integrated Continuous Processes for high quality Biotherapeutics17. Integration of upstream and downstream in continuous biomanufacturing 18. Quality control and regulatory aspects for continuous biomanufacturing19. Continious Validation for Continous Processing20. Validation, uality and Regulatory Considerations in Continuous Biomanufacturing 21. Evaluation of Continuous Downstream processing: Industrial Perspective

Dr. Ganapathy Subramanian is a biotechnology consultant with over 30 years of experience in industry and academia, encompassing the application and development of processing, purification methodologies, and chromatographic systems for large scale use in environmental science, food science, perfumery, cosmetics, and pharmaceuticals. He has also taught extensively in the area of food and medical technology. A chemistry graduate from Madras, India, Dr. Subramanian was awarded his doctorate from the University of Glasgow for work on natural products. His main research interests lie in the utilization of natural material separation processes and bioconversions. Dr. Subramanian has written and edited a number of books and articles in the field of biotechnology. For the last 15 years, he has been organizing conferences promoting the integration and sharing of knowledge between academia and industry.

• 1. Continuous Bioprocess Development: Methods for Control and Characterization of the Biological System2. Tools Enabling Continuous and Integrated Upstream and Downstream Processes in the Manufacturing of Biologicals 3. Engineering Challenges of Continuous Biomanufacturing Processes (CBP) 4. Progress Towards Automated Single Use Continuous Monoclonal Antibody Manufacturing via the Protein Refinery Operations Lab 5. Single-use bioreactors for continuous bioprocessing: challenges and outlook6. Two mutually enabling trends: Continuous bioprocessing and Single-use technologies 7. Perfusion Formats and their specific medium requirements 8. Upstream Continuous Process Development9. Study of Cells in the Steady State Growth Space 10. Continuous Downstream Processing for Production of Biotech Therapeutics11. Evolving Needs For Viral Safety Strategies in Continuous Monoclonal Antibody Bioproduction 12. Multi-Column Continuous Chromatography ? Understanding this enabling Technology13. Continuous Chromatography as a fully integrated process in Continuous Biomanufacturing14. Continuous Chromatography in Biomanufacturing 15. Single Pass Tangential Flow Filtration (SPTFF) in Continuous Biomanufacturing 16. Design of Integrated Continuous Processes for high quality Biotherapeutics17. Integration of upstream and downstream in continuous biomanufacturing 18. Quality control and regulatory aspects for continuous biomanufacturing19. Continious Validation for Continous Processing20. Validation, uality and Regulatory Considerations in Continuous Biomanufacturing 21. Evaluation of Continuous Downstream processing: Industrial Perspective

Dr. Ganapathy Subramanian is a biotechnology consultant with over 30 years of experience in industry and academia, encompassing the application and development of processing, purification methodologies, and chromatographic systems for large scale use in environmental science, food science, perfumery, cosmetics, and pharmaceuticals. He has also taught extensively in the area of food and medical technology. A chemistry graduate from Madras, India, Dr. Subramanian was awarded his doctorate from the University of Glasgow for work on natural products. His main research interests lie in the utilization of natural material separation processes and bioconversions. Dr. Subramanian has written and edited a number of books and articles in the field of biotechnology. For the last 15 years, he has been organizing conferences promoting the integration and sharing of knowledge between academia and industry.

• 1. Continuous Bioprocess Development: Methods for Control and Characterization of the Biological System2. Tools Enabling Continuous and Integrated Upstream and Downstream Processes in the Manufacturing of Biologicals 3. Engineering Challenges of Continuous Biomanufacturing Processes (CBP) 4. Progress Towards Automated Single Use Continuous Monoclonal Antibody Manufacturing via the Protein Refinery Operations Lab 5. Single-use bioreactors for continuous bioprocessing: challenges and outlook6. Two mutually enabling trends: Continuous bioprocessing and Single-use technologies 7. Perfusion Formats and their specific medium requirements 8. Upstream Continuous Process Development9. Study of Cells in the Steady State Growth Space 10. Continuous Downstream Processing for Production of Biotech Therapeutics11. Evolving Needs For Viral Safety Strategies in Continuous Monoclonal Antibody Bioproduction 12. Multi-Column Continuous Chromatography ? Understanding this enabling Technology13. Continuous Chromatography as a fully integrated process in Continuous Biomanufacturing14. Continuous Chromatography in Biomanufacturing 15. Single Pass Tangential Flow Filtration (SPTFF) in Continuous Biomanufacturing 16. Design of Integrated Continuous Processes for high quality Biotherapeutics17. Integration of upstream and downstream in continuous biomanufacturing 18. Quality control and regulatory aspects for continuous biomanufacturing19. Continious Validation for Continous Processing20. Validation, uality and Regulatory Considerations in Continuous Biomanufacturing 21. Evaluation of Continuous Downstream processing: Industrial Perspective