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Forum Overview

China and Asia over the decades has been playing an increasingly important role in the context of clinical research activities due to the significant scientific investment by multinational companies as well as rapidly booming China domestic R&D programs. In past few years, the China regulatory agency has also issued several regulations and initiatives to accelerate the review and approval and improve the quality of new drugs and medical devices. With the joining of ICH in 2017, the government is continuing to improve the regulatory standards and systems to promote innovation, enhance the R&D ecosystem. And the scale, complexity and cost of clinical trials have simultaneously and exponentially increased. However, the drug development is fraught with all kinds of challenges which needs innovation, efficiency and collaboration. 

In return, the Clinical Development and Innovation Forum 2022 will gather leaders and scientists across pharma, biotech and academia for discussions and cases studies on the major topics including: Robust Clinical and Regulatory Strategy, Next Generation Clinical Trials, Oncology and Immuno-Oncology Drug Development, CNS New Drug Development, Clinical Biomarkers and Companion Diagnostics, Cellular Immunotherapy and Gene Therapy Development, Data Science and Digital Innovation, China Domestic R&D Innovation, Innovative Clinical Design and Patient Strategies etc. towards the Efficient and GCP-compliant Drug Development in the era of Precision Medicine.

CDIF2022 Forum Sessions include:

  • Clinical and Regulatory Strategy, Next Generation Clinical Trials
  • Oncology and Immuno-Oncology Drug Development
  • Cellular Immunotherapy, Gene Therapy, Oncolytic Virus Immunotherapy Development
  • CNS Diseases and AutoImmune Diseases Novel Therapey Development
  • Bioanalysis, Biomarkers, Companion Diagnostics and Translational Medicine
  • Biotherapeutics, Bispecific Antibodies and ADC Development
  • China Domestic New Drug Development and Translational Research
  • Innovative Clinical Design and Biostatistics
  • Early and Exploratory Drug Development Strategies
  • Real-world Research, Digital innovation and Virtual Trials
  • AI and Big Data in Drug Development


Currently we are receiving the podium/poster abstracts. If you are working in the above areas, you are invited to submit a proposal. For more information, please contact

Wei Zhang
Program Manager
Organizing Committee
Email: wzhang@deliver-consulting.com
Phone: +86-150-0198-5401