Resources & Media

The new regulations published by the Food and Drug Administration: the Appendix of clinical experimental drugs “Good Manufacturing Quality Management Practice”

February 7, 2023
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GMP2010 Annex——IMP

February 7, 2023
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Clinical Trials Supply in Cell and Gene Therapy

February 7, 2023

Speaker： Susan LI Director, Product Management Thermo Fisher Scientific

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Feasibility proposal for segmented production of biological products —- Based on the exploration of bio-pharmaceutical industry in Suzhou Industrial Zone

January 5, 2023
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Antibody drug cost considerations

January 5, 2023
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CMC development, production and quality control of ADC drugs: challenges and strategy

January 5, 2023
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How to scale manufacturing process using HyPerforma™ DynaDrive™ S.U.B.

December 29, 2022
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Case sharing- how to build a compliant and efficient CGT facility

December 22, 2022
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Challenges in the industrialization of gene and cell therapy

December 22, 2022
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Chinese Webinar丨Data Science Workflows for Process Character

August 18, 2022

Process validation stage 1, also known as process characterization (PCS), is the main step of generating process knowledge that is…

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The ISPE Pharma 4.0™ Operating Model – Basis for the ICH Holistic Control Strategy – An Introduction Webinar

August 11, 2022
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Data Science Tools for Successful Technology Transfer Webinar

August 11, 2022
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