Resources & Media

Exploration on digital application of pharmaceutical supply chain

February 7, 2023
Members Only

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

February 7, 2023
Members Only

GMP2010 Annex——IMP

February 7, 2023
Members Only

Clinical Trials Supply in Cell and Gene Therapy

February 7, 2023

Speaker： Susan LI Director, Product Management Thermo Fisher Scientific

Members Only

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

January 5, 2023
Members Only

Antibody drug cost considerations

January 5, 2023
Members Only

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

January 5, 2023
Members Only

How to scale manufacturing process using HyPerforma™ DynaDrive™ S.U.B.

December 29, 2022
Members Only

Case sharing- how to build a compliant and efficient CGT facility

December 22, 2022
Members Only

Challenges in the industrialization of gene and cell therapy

December 22, 2022
Members Only

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…

Members Only

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

August 11, 2022
Read more
Back To Top