Benchmark Standards & Regulatory Expectations to Confidently Characterise Function, Quality & Potency to Fast-Track Clinical Translation
๐๐จ๐ข๐ง ๐๐จ๐ฎ๐ซ ๐๐ง๐๐ฅ๐ฒ๐ญ๐ข๐๐๐ฅ ๐๐จ๐ฆ๐ฆ๐ฎ๐ง๐ข๐ญ๐ฒ ๐ข๐ง ๐๐จ๐ง๐๐จ๐ง ๐ข๐ง ๐๐๐๐!The inaugural Cell Therapy Analytical Development Summit Europe is the leading industry-defining forum in Europe made exclusively for analytical, CMC, QC, process development and regulatory experts
Next generation cell therapies are emerging as game changing treatments for cancer and beyond, but given their increasing complexities, developing robust, reliable, and in-depth analytical assays is critical to prove their safety and quality to the regulatory authorities
This year we have unrivalled content showcasing:
โข Efforts to harmonise reference standards for state-of-the-art analytical development
โข Regulatory experience case studies to hit guidelines and avoid pushback
โข Strategies to develop a successful potency assay to determine product activity
โข Process transfers demonstrating analytical robustness and product comparability
โข New technology to expand and improve your analytical toolbox
โข Development and validation of analytical methods to fulfil GMP guidelines
โข Best methods to approach final product characterisation by starting with the end in mind
โข Automated technologies for improved accuracy, repeatability and speed
โฆ To provide your team with the lessons learned to achieve success in analytical submissions from IMPD/IND through to the clinic and beyond
Data and learnings will be shared from key European biopharma stakeholders including Cellectis, Gadeta, GSK, and Sanofi and more to support your efforts in developing efficacious, potent and safe cell therapiesUnite with these companies and more this August to fast-track your pipeline into the clinic and beyond
https://cell-therapy-analytics.com/
23-25 August, 2022
8.30am-5pm BST | London, UK
Contact: [email protected]" Target="_BLANK">br>[email protected]
Brochure https://go.evvnt.com/1150433-0?pid=269
Tickets https://go.evvnt.com/1150433-2?pid=269
Category: Conferences | Science, Health & Medicine | Pharmaceuticals
Speakers: Assegid Oumie, Principal Scientist, Analytical Development Lead, Enara Bio, Benoit Champluvier, Executive Director, Process & Analytical Development, Cellectis, Eesha Vyas, Regulatory Affairs Manager, Oncology, ๐๐ฅ๐๐ฑ๐จ๐๐ฆ๐ข๐ญ๐ก๐๐ฅ๐ข๐ง๐, Sharon Longhurst, Vice President of Development, ๐๐๐๐๐ญ๐, Berkan Vural, Cell Analytical Scientist, ๐๐ฅ๐๐ฑ๐จ๐๐ฆ๐ข๐ญ๐ก๐๐ฅ๐ข๐ง๐, Christopher Bravery, Regulatory Scientist, ๐๐ง๐๐๐ฉ๐๐ง๐๐๐ง๐ญ ๐๐จ๐ง๐ฌ๐ฎ๐ฅ๐ญ๐๐ง๐ญ, Jeetendra Kumar, Specialist R&D, ๐๐ฆ๐ฆ๐ฎ๐ง๐๐๐ฅ ๐๐ก๐๐ซ๐๐ฉ๐๐ฎ๐ญ๐ข๐๐ฌ, Sofia Hรฅkansson Buch, Vice President, Cell Therapy CMC, ๐๐จ๐ฏ๐จ ๐๐จ๐ซ๐๐ข๐ฌ๐ค, Arindam Mitra, Associate Director, CMC, ๐๐๐ฎ๐๐ข๐ ๐๐ข๐จ, Chaya Mazouz, Vice President, Quality (IL) & Global Regulatory Affairs, ๐๐ซ๐ ๐๐ง๐๐ฌ๐ข๐ฌ, Driss Chader, Analytical Development Engineer, ๐๐๐ฅ๐ฅ๐๐๐ญ๐ข๐ฌ, Farzin Farzaneh, Chair of Molecular Medicine, ๐๐ข๐ง๐ โ๐ฌ ๐๐จ๐ฅ๐ฅ๐๐ ๐ ๐๐จ๐ง๐๐จ๐ง, Adi Zohar, Quality Control Manager, ๐๐ฅ๐ฎ๐ซ๐ข๐ฌ๐ญ๐๐ฆ ๐๐ก๐๐ซ๐๐ฉ๐๐ฎ๐ญ๐ข๐๐ฌ, Ruti Goldberg, Compliance & Methods Validations Manager, ๐๐ฅ๐ฎ๐ซ๐ข๐ฌ๐ญ๐๐ฆ ๐๐ก๐๐ซ๐๐ฉ๐๐ฎ๐ญ๐ข๐๐ฌ, Yvet Noordman, Head of Analytical Development, Bioanalytics Genomic Medicine, ๐๐๐ง๐จ๐๐ข, Hรฉlรจne Negre, EPFIA Project Leader, ๐๐๐๐ฏ๐จ๐ฅ๐ฏ๐ ๐๐๐ ๐๐จ๐ง๐ฌ๐จ๐ซ๐ญ๐ข๐ฎ๐ฆ, ๐๐๐ซ๐ฏ๐ข๐๐ซ, Mohamad Toutounji, ADQC Scientist, Cell Therapy, ๐๐๐ง๐จ๐๐ข, Terri Gaskell, Chief Technology Officer, ๐๐ข๐ง๐ซ๐ข ๐๐ก๐๐ซ๐๐ฉ๐๐ฎ๐ญ๐ข๐๐ฌ, Emilio Cosimo, Product Development Manager, ๐๐ ๐๐ข๐จ๐๐ก๐๐ซ๐ฆ, Katherine Cornish, Senior Stem Cell Biologist, Head of Cell Therapy, ๐๐ ๐๐ญ๐๐ฆ ๐๐๐ฅ๐ฅ ๐๐๐ง๐ค, ๐๐๐๐๐, Therese Choquette, Head of Analytical Science, ๐๐ข๐ ๐๐ง ๐๐ก๐๐ซ๐ฆ๐
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