Operational information
This data is publicly available. Parent page : ION-2197
Operational data for China Marrow Donor Program - ION-2197 | |
|---|---|
| Organisation Overview | |
| The information has been reviewed in year : | |
| Issuing organisation Number (ION) | ION-2197 The Issuing Organisation Number of a organisation, this is globally unique number, as issued by the ICCBBA. |
| Time zone | Asia/Hong_Kong (GMT+08:00) The timezone in which this organisation operates. |
| Business hours | 08:30-11:30 13:30-17:00 The daily hours in which this organisation operates. |
| Work schedule | Monday through Friday The normal work week in which this organisation operates. |
| Organisation closures | For all organisation closures, please see the WMDA Calendar. |
| Donor ID example | 123456789012 ID to be expected on paperwork, samples, and products. |
| Preliminary Search | |
| Requires preliminary search request form | Yes If yes, form required can be found on the Documents Page. |
| Extended Typing | |
| Typing options available for request | Please note special requirements listed |
| Requires organisation specific typing request form | No If yes, form required can be found on the Documents Page. |
| Number of days donor is reserved for a patient after a request | 90 days |
| Verification Typing | |
| Maximum blood volume allowed | 30 mls |
| Requires organisation specific typing request form | No If yes, form required can be found on the Documents Page. |
| IDM testing performed at verification | No |
| Number of days donor is reserved for a patient after a request | 90 days |
| Sibling Typing | |
| Registry is willing to arrange sibling typings | No |
| If yes, procedure to apply for sibling typings | |
| Workup Request | |
| Product dosage limit | PBSC : ≥5×10,8/Kg , CD34+:≥2×10,6/Kg Number of donor cells allowed based on recipient weight. |
| Requires patient to meet certain standards in order to proceed with collection | No Organisation may or may not allow donor collections for some patients. |
| Patient physician must report the following in order to proceed with collection | Yes, patient physician needs to provide patient report on status and treatment plan. Must provide additional information to organisation. |
| Requires organisation specific work up forms | Yes If yes, form(s) required can be found on the Documents Page. |
| Workup IDM completed 30 days prior to collection | Yes Donor IDM results must be performed within 30 days of collection date to be valid and allow the collection to proceed. |
| Medical Health Questionnaire example available | Yes If yes, the example can be found on the Documents Page. |
| Post-Transplant | |
| Subsequent donation policy | For DLI, after 1 months; for PBSC, after 3 months |
| Anonymous contact allowed | at least 2 year after collection/transplantation |
| Direct contact allowed | No. |
| Gift exchange allowed | Small gift through CMDP. |
| Cord blood contact allowed | N/A |
Regulatory information
IDM
| IDM | Tested | Method | Days between test and sampling/workup |
|---|---|---|---|
| ALT/ASTALT/AST ratio, De-Ritis-Quotient | - | ||
| ChagasChagas, T. cruzi | - | ||
| CMV IgGCytomegalovirus (CMV) Antibody testing IgG | Yes | ||
| CMV IgMCytomegalovirus (CMV) Antibody testing IgM | Yes | ||
| CMV TotalCytomegalovirus Total | Yes | ||
| EBV IgGEpstein-Barr Virus Antibody testing IgG | On request | ||
| EBV IgMEpstein-Barr Virus Antibody testing IgM | On request | ||
| HAV (NAT)Anti-hepatitis A virus nucleic acid testing | Yes | ||
| HBV (NAT)Hepatitis B nucleic acid testing | On request | ||
| HBc AbHepatitis B core antibody testing | Yes | ||
| HBs AgHepatitis B Surface antigen testing | Yes | ||
| HCV (NAT)Hepatitis C nucleic acid testing | Yes | ||
| HCV AbHepatitis C antibody testing | Yes | ||
| HEV (NAT)Hepatitis E Virus nucleic acid testing | On request | ||
| HIV (NAT)Human Immunodeficiency Virus nucleic acid testing | On request | ||
| HIV-1 AbHuman Immunodeficiency Virus HIV-1 antibody testing | Yes | ||
| HIV-2 AbHuman Immunodeficiency Virus HIV-2 antibody testing | Yes | ||
| HIV p24Human Immunodeficiency Virus p24 antigen testing | On request | ||
| HTLV-IHuman T-Lymphotropic Virus type I testing | On request | Donor samples will be provided for HTLV testing on request from the requesting registry. | |
| HTLV-IIHuman T-Lymphotropic Virus type II testing | On request | Donor samples will be provided for HTLV testing on request from the requesting registry. | |
| MalariaMalaria | - | ||
| HSVHerpes Simplex Virus | - | ||
| STSSerological tests for syphilis | Yes | ELISA | |
| STS FTA-ABSSerological test for syphilis | Yes | ||
| ToxoplasmosisToxoplasmosis | - | ||
| VZVVaricella Zoster Virus | - | ||
| WNV-NATWest Nile Virus nucleic acid testing | On request | ||
| Other tests performed | On request |
Comment
Donors requested for international exchange will be tested for ABO/Rh at the time of verification typing.
The data provided on this page is updated by the organisations.
The WMDA makes no representations or express or implied warranties regarding any information on this page.
Use of any information provided on this site does not and is not intended to create a contractual or other relationship.
The WMDA makes no representations or express or implied warranties regarding any information on this page.
Use of any information provided on this site does not and is not intended to create a contractual or other relationship.
General | |
|---|---|
| The information has been reviewed in year : | |
| Organisation name: | China Marrow Donor Program |
| Organisation ION: | ION-2197 |
| Country: | China |
| Year the registry started operations: | 2001 |
Products | comment | |
|---|---|---|
| Do you provide HPC, Marrow? | no | |
| Do you provide HPC, Apheresis? | yes | |
| Do you provide HPC, Cord Blood? | no | |
| Do you provide MNC, Apheresis? | no | |
| Do you provide NC, Whole Blood? | no | |
Product quantity | ||
|---|---|---|
| Data valid for year | 2024 | |
| Number of products | National | International |
| HPC, Marrow products: | 0 | 0 |
| HPC, Apheresis: | 2470 | 19 |
| HPC, Cord: | 0 | 0 |
License | |
|---|---|
| Organisation is licensed/accredited by the Health Authority: | yes |
| Comment: | |
| Name of Health Authority: | Red Cross Society of China |
| Date of last inspection: | |
| Link to website of Health Authority: | https://www.redcross.org.cn/ |
| Can you provide the Legal documentation from the Competent Authority that your organisation is allowed to operate as a registry ? | yes |
| The registry is accredited by any other organisation: | no |
| If yes, by which organisation? | |
Donor policy | |
|---|---|
| All donors are unpaid volunteers: | yes |
| All donors are informed about donation process and associated risks: | yes |
| Donors sign a valid informed consent to donate in the presence of a medical doctor/health care personnel/registry staff: | yes |
| The registry has systems in place to protect and control access to donor/patient records: | yes |
| The registry maintains donor anonymity: | yes |
| The registry has detailed donor evaluation and exclusion criteria in place: | yes |
| The registry has donor evaluation and exclusion criteria that do meet or exceed the WMDA guidelines: | yes |