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These data are submitted by the = cord blood bank to the WMDA in February 2015. The WMDA makes no representat= ions or express or implied warranties regarding any information on this sit= e or obtained through these links; expressly disclaims all legal liability = and responsibility for the accuracy, completeness, currency, suitability, v= alidity, or usefulness of such information; and is not and will not be liab= le for any statements, errors, or omissions in posted information, or for a= ny losses, injuries, or damages that arise or are alleged to arise from suc= h information. Use of any information provided on this site does not and is= not intended to create a contractual or other relationship. All informatio= n is on an as-is basis. The data cannot be updated.
1. General Information | |
---|---|
Name of CBB | ERCB ( Emilia Romagna Cord Blood Bank) |
CBB Director | Claudio |
CBB Director | Velati |
Address | via Massarenti 9 |
Address | 40138 |
Address | Bologna |
Phone Number | +39 051 2143011 |
Date CBB Started Collecting C=
ord Blood Units (month/day= /year) |
11/01/1997 |
Number of Public Cord Blood U= nits | 4,606 |
Planned Number of Public Cord= Blood Units Stored in 2015 | 300 |
Lists on BMDW | Yes |
Affiliated with National Stem= Cell Donor Registry | No |
2. Cord Blood Units in Inventory | |
Current Processing Method | Liquid+ red auto |
Current Processing Method | Vapour+ red auto |
Previous Processing Method= td> | Liquid- red manual |
Previous Processing Method= td> | Liquid- plasma only |
Year Current Process Method = Started | 2007 |
Percent of Units Plasma and = RBC Reduced (manual) | 5 |
Percent of Units Plasma and = RBC Reduced (automated) | 43 |
Percent of Units No Volume R= eduction | 52 |
3. Accreditations, Licenses and Certifications= th> | |
FACT-Netcord | Yes |
AABB | No |
Competent Authority/ Nationa= l Health Authority | Yes |
Name of Competent Authority<= /td> | National Blood Center ( Italian Ministery of hea= lth) |
ISO | No |
4. Cord Blood Collection | |
Current Collection Practice<= br>Is the collection In/Ex -U= tero or both? | In-utero |
Current Antiseptic | Chlorhexidine |
Collection Bag | Double needle |
Agitation during Collection<= /td> | Manual |
5. Conditioning/Transport from Collection Site t= o CBB | |
Secondary Bag Used | Yes |
Transport Conditions | Qualified transporter |
Transport Conditions | Insulating transport container |
Transport Conditions | Passive refrigeration system |
Temp. for Storage and Transp= ort | Other (lower limit +1-35=C2=B0C, higher limit +6= -30=C2=B0C) |
6. Pre-Processing Evaluation | |
Completed Prior to Accepting= a CBU | Medical history, collection report, informed con= sent |
Current Threshold for Accept= ing a CBU | Viability threshold CD45 |
Method for CD34 Remuneration= | ISHAGE guidelines |
External Proficiency Testing= for QC of FACS Lab | UKNEQAS |
Post Processing/ Pre Freeze = CD34+ Cell Count | Yes |
Time from Collection to Proc= essing | up to 48H |
7. Processing and Packaging | |
Pre Freeze Processing Method= s- Unit in Inventory | SEPAX |
Pre Freeze Processing Method= s- Current | SEPAX |
Additives Currently in Use= td> | HES |
Current Cryopreservation Met= hod | Conventional CRF |
Current Cryoprotectant Addit= ive | Ready for use DMSO-Dextran |
Current Cryobag | Single bag (one fraction) |
Current Target Cryopreservat= ion Volume (mL) | 26.5 |
Current Packaging for Storag= e | Overwrap |
Current Packaging for Storag= e | Canister |
Current Packaging for Storag= e | More than one segment |
Current Packaging for Storag= e | Additional separate segments |
8. Testing | |
PCR Performed on IgM+ Result= | CMV |
PCR Performed on IgM+ Result= | EBV |
Extra Material Currently Sto= red | Cord blood DNA |
Extra Material Currently Sto= red | Cord blood material for DNA extraction |
Extra Material Currently Sto= red | Plasma/cord blood |
Extra Material Currently Sto= red | Maternal material for DNA extraction |
Extra Material Currently Sto= red | Maternal plasma/serum |
Current Post Processing Thre=
shold for Accepting a CBU for Public Use TNC |
120 |
Current Post Processing Thre=
shold for Accepting a CBU for Public Use CD34 (10^6) Single Platform |
NA |
Current Post Processing Thre=
shold for Accepting a CBU for Public Use CFU-GM |
NA |
Current Post Processing Thre=
shold for Accepting a CBU for Public Use CFU |
NA |
Current Post Processing Thre=
shold for Accepting a CBU for Public Use Viability |
80 |
9. Storage | |
Type of Storage Container Us= ed | Conventional tank liquid phase |
Monitoring of Storage | Centralized system remote monitoring |
Monitoring of Storage | LN2 level |
Monitoring of Storage | Lid opening |
Monitoring of Storage | System default |
Monitoring of Storage | Temperature monitoring |
10. HLA Typing | |
Current Level of HLA Typing =
at Time of Listing HLA-A <= /span> |
LR |
Current Level of HLA Typing =
at Time of Listing HLA-B <= /span> |
LR |
Current Level of HLA Typing =
at Time of Listing HLA-C <= /span> |
LR |
Current Level of HLA Typing =
at Time of Listing HLA-DRB= 1 |
HR |
Current Level of HLA Typing =
at Time of Listing HLA-DQB= 1 |
|
Current Level of HLA Typing =
at Time of Listing HLA-DPB= 1 |
|
Accreditation of HLA Lab | EFI accredited lab |
Average Turnaround Time for =
Extended HLA Typing Results in days |
?10 |
Attached Segment Used for Co= nfirmatory/ Verification Typing | Yes |
Units Listed without Attache= d Segment and have not been Previously Typed on Attached Segment | Yes |
Percentage of CBUs that have= an Attached Segment | 50-75% |
Confirmatory/ Verification T= yping on an Attached Segment is Pre-Release Requirement | Yes |
11. Reservation and Cancellation Policies | |
What Point is a CBU Reserved= for a Patient | Reservation request |
Length of Time a CBU can be =
Reserved in days | 30 |
Reservation Fee | No |
Reservation Cancellation Fee= in Absence of Shipment Request | No |
Can Reservation be Extended<= /td> | Yes |
Is a Unit Report Provided on= a Unit that is Reserved for Another Patient | No |
Is TC Informed when CBU is R= eleased | Yes |
12. Release and Shipment | |
Hemoglobinopathy Screening P= erformed Prior to Release | Yes |
Criteria to Ship a CBU |
40 |
Criteria to Ship a CBU |
Yes |
Current Packaging for Shipme= nt to TC | Metal canister |
Current Packaging for Shipme= nt to TC | Overwrap |
Current Packaging for Shipme= nt to TC | Transport rack |
Time Between Shipment Reques= t and Sending CBU | 2-3 weeks |
Fee for Shipment Cancellatio= n | No |
Dry Shippers Validated to Ma= intain Temperature of at least -150 for 48 hours Beyond Expected Arrival | Yes |
Electronic Temperature Data = Logger on All Dry Shippers | Yes |
Who Selects Transport Compan= y | CBB |
Who Selects Transport Compan= y | World courier |
Shape of Transport Container= | Cubic |
13. Adverse Events Reporting | |
Who are S(P)EARS Reported To=
Competent Authority |
Yes |
Who are S(P)EARS Reported To=
Internal Report = td> | Yes |
Who are S(P)EARS Reported To=
National Registry = |
Yes |
Who are S(P)EARS Reported To=
Transplant Center<= /td> | Yes |
Who are S(P)EARS Reported To=
WMDA |
Yes |