ReviewAdvances in experimental medicine and biology2025
Challenges and Prospects for Cell Therapy Regulation in China.
Review in Advances in experimental medicine and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The development of advanced cell-based intervention in China has been rapid, yet it faces a multitude of regulatory challenges. This article comprehensively analyzes the current state and developmental trajectory of the regulatory framework for advanced cell-based intervention in China. The regulation of stem cells and other cell-based interventions in China has undergone multi-phase development, resulting in a relatively well-established regulatory framework that emphasizes pre-clinical research, Good Manufacturing Practices (GMP), and stringent review processes. However, the jurisdiction still confronts several challenges in advanced cell-based intervention regulation. To address these challenges, future regulatory directions in China may include clarifying the drug status of advanced cell-based intervention products, improving technical evaluation systems, establishing risk classification and tiered management systems, strengthening ethical review mechanisms, enhancing the standardization of clinical research, optimizing industrial chain links, and establishing knowledge-sharing platforms.
Indexed as
Identifiers
41136832What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.