
Event title:Cell Culture & Cell Therapy: Bioprocessing Conference
Dates:26 -27 June 2017
Venue:Philadelphia, USA
Description:
Cellular therapies hold the potential to revolutionize health care for a variety of diseases. However, the limitations lie in the productivity of engineered cells and the safe, efficacious and cost effective transformation of commercialized cell therapies. The industry is yet to address certain gaps relating to these limitations that will facilitate clinical and commercial success of these therapies. The aim of the conference is to assess the risks and benefits of the cell culture and cell therapy bio-manufacturing by focusing in particular on the feasibility of process automation: its impact on regulatory compliance and return on investment.
MarketsandMarkets has put together a unique platform to establish the reproducible and robust manufacturing processes for the production of stable cell culture and therapeutic cells. At the Cell Culture & Cell Therapy: Bioprocessing Conference scheduled to be held in Philadelphia, USAon 26 - 27 June 2017, leading experts in the industry will be gathered to discuss strategies, technologies and innovations in the area of bioprocessing of cell culture and cell-gene therapies.
Target Audience: From Pharmaceuticals, biopharmaceuticals and therapeutics based companies –
Engineers/Scientists/Researchers/Project leaders/VPs/Heads in:
• Bioprocess development • Cellular Therapy • Gene Therapy • Therapeutics • Pharmacology |
• Quality Control • Biotherapeutics • Cell Engineering • Regulatory affairs • Therapeutics |
From Universities and Research Institutes:
Scientists/Professors/Researchers/Project leaders in
• Bioprocessing • Biochemistry • Bioengineering • Biomaterials • Chemical Engineering • Molecular Biology • Material Sciences |
• Pharmacology • Biotechnology • Cell therapy • Gene therapy • Cell culture • Cell Engineering |
Key Sessions
• Fermentation technologies
• Device technologies for bioprocessing of cell culture
• Next generation cellular models
• Optimization of cell culture process
• Closed system manufacturing of cells
• Process development for next generation bio-therapeutics
• Ex-vivo gene therapy application
• Compatibility and stability of cell therapy products
• Automation process development and control
• C-GMP compliance guidelines
• FDA approvals and regulatory policies
• Commercialized view of bioprocessing
• Insurance and reinvestment policies
URL:
Contact Information:
Contact Person – Ajay Nimbalkar