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pericyte therapy

pericyte therapy, Total:43 items.

The international standard classification for "pericyte therapy" includes: Medical Sciences and health care facilities in general , Biology. Botany. Zoology , Medical materials .

The Chinese standard classification for "pericyte therapy" includes: Sanitation in general , Biological agent and blood products , Extracorporeal circulation, artificial organ and prosthesis device , Medical apparatus and devices in general .


Group Standards of the People's Republic of China

  • T/CEAC 105-2025 TIL Cell Therapy Clinical Application Guidelines
  • T/SBX 055-2022 Test methods for tumorigenicity of stem cell therapy products
  • T/CSCB 0019-2024 Stem Cell Marker Molecular Detection Flow Cytometry
  • T/SHSYCXH 8-2022 Test method of human Natural Killer cells and Natural Killer T cells from peripheral blood-Flow cytometry
  • T/CEAC 069-2024 Cell therapy Leukopak raw material collection and immune cell separation technical requirements
  • T/CEAC 059-2024 General requirements for detection of circulating tumor cells in peripheral blood
  • T/SHSYCXH 13-2024 Detection of Regulatory T Cells in Peripheral Blood of Humans by Flow Cytometry
  • T/CMBA 011-2020 Collection, Separation and Preservation of PBMC from Human Peripheral Blood
  • T/SHSYCXH 14-2024 Detection of Neutrophils and nCD64 Index in Peripheral Blood by Flow Cytometry
  • T/CSBM 0044-2023 Non-antibody-dependent magnetic separation detection method of circulating tumor cells in peripheral blood
  • T/SHSYCXH 7-2022 Test method of human monocyte populations from peripheral blood-Flow cytometry

Professional Standard - Hygiene

  • WS/T 360-2011 Guidelines for peripheral lymphocyte subsets by flow cytometry
  • WS/T 360-2024 Guideline for enumeration of peripheral blood lymphocyte subsets by flow cytometry
  • WS/T 245-2005 Reference method for the enumeration of erythrocytes and leucocytes

National Health Commission of the People's Republic of China

  • WST 360:2011 Guidelines for detection of peripheral blood lymphocyte subsets by flow cytometry

Professional Standard - Agriculture

  • 150药典 三部-2020 Monograph Ⅱ Therapeutic topical human granulocyte macrophage stimulating factor gel
  • 149药典 三部-2020 Monograph II Therapeutic Human Granulocyte Macrophage Stimulating Factor for Injection
  • 118药典 三部-2010 Chapter II Therapeutic Recombinant Human Granulocyte Macrophage Stimulating Factor for Injection
  • 142药典 三部-2015 Monograph II Therapeutic Recombinant Human Granulocyte Macrophage Stimulating Factor for Injection

Jilin Provincial Standard of the People's Republic of China

  • DB22/T 2853-2017 Peripheral Blood High Fluorescence Intensity Lymphocyte Percentage (HFLC%) Screening Technical Regulations for Atypical Lymphocytes

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB/T 39729-2020 General requirements for measurement of cell purity—Flow cytometry
  • GB/T 39730-2020 General requirements for cell counting—Flow cytometry

Professional Standard - Medicine

  • YY/T 0606.13-2008 Tissue Engineered Medical Product - Part 13: Standard Test Method for Automated Enumeration of Cell Suspensions
  • YY/T 1465.6-2019 Immunogenic evaluation method of medical devices―Part 6:Determination of animal spleen lymphocyte subsets by flow cytometry
  • YY/T 1465.4-2017 Immunogenic evaluation method of medical devices-Part4:Phagocytosis of mouse peritoneal macrophages on chicken erythrocytes- Ex-vivo method

Shanghai Provincial Standard of the People's Republic of China

  • DB31/T 687-2013 Basic requirements for clinical cell therapy platform settings

Hebei Provincial Standard of the People's Republic of China

  • DB13/T 5332-2021 Technical specification for clinical operation of cellular immunotherapy

GCC Standardization Organization

  • GSO ASTM F3206:2022 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies

Kingdom of Bahrain Testing and Metrology Directorate

  • BH GSO ASTM F3206:2023 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies

American Society for Testing and Materials (ASTM)

  • ASTM F3206-25 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
  • ASTM F3206-17 Standard Guide for Assessing Medical Device Cytocompatibility with Delivered Cellular Therapies
  • ASTM F3368-19 Standard Guide for Cell Potency Assays for Cell Therapy and Tissue Engineered Products
  • ASTM D3576-20 Standard Test Method for Cell Size of Rigid Cellular Plastics
  • ASTM F895-25 Standard Test Method for Agar Diffusion Cell Culture Screening for Cytotoxicity
  • ASTM D3576-25 Standard Test Method for Cell Size of Rigid Cellular Plastics

British Standards Institution (BSI)

  • BS PAS 84:2012 Cell therapy and regenerative medicine. Glossary
  • BS PAS 83:2006 Guidance on codes of practice, standardised methods and regulations for cell-based therapeutics
  • BS EN 30993-5:1994 Biological evaluation of medical devices-Tests for cytotoxicity, in vitro methods
  • BS ISO 20391-1:2018 Biotechnology. Cell counting. General guidance on cell counting methods

Clinical and Laboratory Standards Institute

  • NCCLS H7-A3-2000 Procedure for determination of hematocrit by microhematocrit method

American National Standards Institute (ANSI)

Korean Agency for Technology and Standards (KATS)

  • KS P 1600-2018(2023) General guideline of safety test for the cell based therapeutic substances
  • KS P 1600-2023 General guideline of safety test for the cell based therapeutic substances