Skip to end of metadata
Go to start of metadata

CBB Survey 2015

These data are submitted by the cord blood bank to the WMDA in February 2015. The WMDA makes no representations or express or implied warranties regarding any information on this site or obtained through these links; expressly disclaims all legal liability and responsibility for the accuracy, completeness, currency, suitability, validity, or usefulness of such information; and is not and will not be liable for any statements, errors, or omissions in posted information, or for any losses, injuries, or damages that arise or are alleged to arise from such information. Use of any information provided on this site does not and is not intended to create a contractual or other relationship. All information is on an as-is basis. The data cannot be updated.


1. General Information
Name of CBBSanquin CBB
CBB DirectorJacqueline
CBB DirectorVan Beckhoven
AddressPlesmanlaan 1B
Address2333BZ
AddressLeiden
Phone Number+31715685300
Date CBB Started Collecting Cord Blood Units
(month/day/year)
09/01/1994
Number of Public Cord Blood Units3,539
Planned Number of Public Cord Blood Units Stored in 2015600
Lists on BMDWYes
Affiliated with National Stem Cell Donor RegistryYes
Registry AffiliationEuropdonor Foundation
2. Cord Blood Units in Inventory
Current Processing MethodLiquid+ red auto
Previous Processing MethodLiquid+ red manual
Previous Processing MethodLiquid- red manual
Year Current Process Method Started2008
Percent of Units Plasma and RBC Reduced (manual)25
Percent of Units Plasma and RBC Reduced (automated)70
Percent of Units No Volume Reduction5
3. Accreditations, Licenses and Certifications
FACT-NetcordYes
AABBNo
Competent Authority/ National Health AuthorityYes
Name of Competent AuthorityInspectie voor de Gezondheids Zorg
Audited by National Stem Cell RegistryYes
ISOYes
4. Cord Blood Collection
Current Collection Practice
Is the collection In/Ex -Utero or both?
In-utero
Current AntisepticBetadine
Collection BagDouble needle
Agitation during CollectionManual
5. Conditioning/Transport from Collection Site to CBB
Secondary Bag UsedYes
Transport ConditionsQualified transporter
Temp. for Storage and TransportRoom temperature
6. Pre-Processing Evaluation
Completed Prior to Accepting a CBUMedical history, collection report, informed consent
Method for CD34 RemunerationISHAGE guidelines
External Proficiency Testing for QC of FACS LabUKNEQAS
Post Processing/ Pre Freeze CD34+ Cell CountYes
Time from Collection to Processingup to 48H
7. Processing and Packaging
Pre Freeze Processing Methods- Unit in InventoryAXP
Pre Freeze Processing Methods- Unit in InventoryNo processing
Pre Freeze Processing Methods- Unit in InventoryVolume reduction with HES-Manual
Pre Freeze Processing Methods- Unit in InventoryOther: Ficoll sedimentation
Pre Freeze Processing Methods- CurrentAXP
Additives Currently in UseNo additive
Current Cryopreservation MethodBioArchive
Current Cryoprotectant AdditiveDMSO
Current CryobagSingle bag 80:20
Current Target Cryopreservation Volume (mL)25.0
Current Packaging for StorageOverwrap
Current Packaging for StorageCanister
Current Packaging for StorageMore than one segment
8. Testing
Extra Material Currently StoredCord blood DNA
Extra Material Currently StoredCord blood material for DNA extraction
Extra Material Currently StoredPlasma/cord blood
Extra Material Currently StoredMaternal material for DNA extraction
Extra Material Currently StoredMaternal plasma/serum
Current Post Processing Threshold for Accepting a CBU for Public Use
TNC
100
Current Post Processing Threshold for Accepting a CBU for Public Use
CD34 (10^6) Single Platform
NA
Current Post Processing Threshold for Accepting a CBU for Public Use
CD34 (10^6) Double Platform
NA
Current Post Processing Threshold for Accepting a CBU for Public Use
CFU-GM
NA
Current Post Processing Threshold for Accepting a CBU for Public Use
CFU
NA
Current Post Processing Threshold for Accepting a CBU for Public Use
Viability
80
9. Storage
Type of Storage Container UsedBioArchive
Type of Storage Container UsedDouble walled liquid nitrogen
Monitoring of StorageCentralized system remote monitoring
Monitoring of StorageLN2 level
Monitoring of StorageTemperature monitoring
10. HLA Typing
Current Level of HLA Typing at Time of Listing
HLA-A
IR
Current Level of HLA Typing at Time of Listing
HLA-B
IR
Current Level of HLA Typing at Time of Listing
HLA-C
IR
Current Level of HLA Typing at Time of Listing
HLA-DRB1
HR
Current Level of HLA Typing at Time of Listing
HLA-DQB1

Current Level of HLA Typing at Time of Listing
HLA-DPB1

Accreditation of HLA LabEFI accredited lab
Average Turnaround Time for Extended HLA Typing Results
in days
9
Attached Segment Used for Confirmatory/ Verification TypingYes
Units Listed without Attached Segment and have not been Previously Typed on Attached SegmentYes
Percentage of CBUs that have an Attached Segment75-90%
Confirmatory/ Verification Typing on an Attached Segment is Pre-Release RequirementYes
11. Reservation and Cancellation Policies
What Point is a CBU Reserved for a PatientHLA typing request
Length of Time a CBU can be Reserved
in days
90
Reservation FeeNo
Reservation Cancellation Fee in Absence of Shipment RequestNo
Can Reservation be ExtendedYes
Is a Unit Report Provided on a Unit that is Reserved for Another PatientNo
Is TC Informed when CBU is ReleasedNo
12. Release and Shipment
Hemoglobinopathy Screening Performed Prior to ReleaseYes
Criteria to Ship a CBU
Viability and Cell Count
50
Criteria to Ship a CBU
HLA Identity Testing
Yes
Current Packaging for Shipment to TCMetal canister
Current Packaging for Shipment to TCOne attached segment
Current Packaging for Shipment to TCOverwrap
Time Between Shipment Request and Sending CBU4 days-1 week
Fee for Shipment CancellationYes
Dry Shippers Validated to Maintain Temperature of at least -150 for 48 hours Beyond Expected ArrivalYes
Electronic Temperature Data Logger on All Dry ShippersYes
Who Selects Transport CompanyRequesting transplant centre
Shape of Transport ContainerOther
Shape of Transport ContainerBoth Cubic and Mushroom
13. Adverse Events Reporting
Who are S(P)EARS Reported To
Competent Authority
Yes
Who are S(P)EARS Reported To
National Registry
Yes

14. Pictures of cord blood units in the inventory


15. Infectious Disease Marker (IDM) CURRENTLY performed.



Holiday Calendar

  1. EDIT THE CALENDAR

    Customize the different types of events you'd like to manage in this calendar.

    #legIndex/#totalLegs
  2. RESTRICT THE CALENDAR

    Optionally, restrict who can view or add events to the team calendar.

    #legIndex/#totalLegs
  3. SHARE WITH YOUR TEAM

    Grab the calendar's URL and email it to your team, or paste it on a page to embed the calendar.

    #legIndex/#totalLegs
  4. ADD AN EVENT

    The calendar is ready to go! Click any day on the calendar to add an event or use the Add event button.

    #legIndex/#totalLegs
  5. SUBSCRIBE

    Subscribe to calendars using your favorite calendar client.

    #legIndex/#totalLegs

  • No labels