DISCOVER WHAT REALLY MAKES A DIFFERENCE IN CHOOSING A BIOBANK

Processing and cryopreservation

When it comes to cord blood preservation, the focus often shifts solely to the final stage: the freezing of the sample. But what truly makes a difference happens much earlier: the PROCESSING of the biological material (blood, cord, and placenta).
It is during this phase that the sample is processed, tested, and prepared for cryopreservation.

The future quality of the cells, and thus their actual clinical usability, depends precisely on this KEY phase. SSCB is the only Swiss company that guarantees processing and storage are done in Switzerland in compliance with FACT-NetCord standards and authorized by Swissmedic, unlike our main competitors who process the sample abroad. For a comparison between SSCB and the competitors/distributors of foreign companies, see the comparison table available on this page.

the guidelines

What do international standards say?

FACT–NetCord

The global clinical standard specific to cord blood, with stringent requirements for collection, processing, and storage, ensuring inclusion in international transplant registries (and thus the actual usability of the sample in a transplant context)
factglobal.org, parentsguidecordblood.org

AABB

A more "generic" standard for process and traceability, useful for operational quality, but which does not ensure the same level of clinical acceptance in transplant registries: this means that a unit certified only by AABB may not be usable when it is truly needed
cord.memberclicks.net, parentsguidecordblood.org

PROCESSING is an active and critical phase, requiring controlled environments, highly qualified personnel, and strict protocols.

CRYOPRESERVATION, on the other hand, is a passive phase: it only works if the processing has been done correctly.

The value of SSCB

Control, transparency, quality

Swiss Stem Cells Biotech (SSCB) is the only private biobank in Switzerland that manages the entire process – from processing to cryopreservation – in its own laboratories in Switzerland, accredited by FACT–NetCord for cord blood, and GMP certified for cord tissue and placenta.

Why Choose Swiss Stem Cells Biotech?

What are our competitors really doing?

Many companies present themselves as “Swiss” but do not have their own laboratories in the country. For this reason:

The biological material (blood, cord, placenta) is transported abroad after collection (for example, to Poland, England, Portugal, etc.).

Abroad, it is processed and frozen, according to the standards of that country and not according to Swissmedic standards.

Only later are the samples returned to Switzerland, in bulk (not individually), for storage, with associated transportation risks.

SSCB guarantees you a 100% Swiss process.

We have been active for over 20 years and we offer you:

Processing and cryopreservation in Switzerland

Immediate and complete traceability

SSCB-owned laboratories certified GMP and Fact-NetCord

No overseas transfer

Biological material (blood, cord tissue, placenta) waste regulated according to Swissmedic provisions.

Regarding the processing phases, unlike its main competitors, SSCB is regularly inspected by Swissmedic and every three years by independent auditors from FACT-NETCORD, ensuring absolute quality for all our clients.

The Hybrid Solution

SSCB is the only private biobank in Switzerland authorized to offer the hybrid banking model, thanks to its presence across the country and its certifications.

This is made possible by a pilot project approved by the Federal Office of Public Health (FOPH) and implemented in partnership with:

– Swiss Blood Stem Cells of Transfusion (CRS) Switzerland
– Bern University Hospital
– Canton Hospital Authority Ticino EOC

Public Storage

If parents choose to donate, the stem cells will no longer be available to the family. In case of need, they must consult the public registry to check the availability of compatible cells.

Private Storage

A choice that protects the family: the stored cells are reserved exclusively for the child or their relatives, ensuring maximum safety for their health. While the service requires a financial contribution, it offers a valuable opportunity for the family's future.

NEW: Hybrid Storage

The most complete option: stem cells are stored for family use but can be donated upon request. In the event of a transplant donation, the storage costs are reimbursed. A choice that combines family protection with solidarity, with the final decision always in the hands of the family.

Corded fabric

specific requirements are needed (and we have them)

According to Swiss jurisprudence and the Federal Office of Public Health (FOPH), the processing of cord tissue is subject to specific criteria:

GMP (Good Manufacturing Practice) compliant environments

Aseptic production in controlled conditions

Official operating authorization issued by Swissmedic and use of certified laboratories

SSCB is fully compliant with all these requirements. In our laboratories in Switzerland, we process and cryopreserve cord tissue according to the required standards, without any foreign outsourcing.

Comparison table between SSCB and other operators present in Switzerland (e.g. Famicord Suisse SA and Future Health)

Appearance
SSCB – Swiss Stem Cells Biotech
Other operators present in Switzerland (e.g. Famicord Suisse SA and Future Health)
Processing
Takes place in Switzerland, in the GMP-certified SSCB-owned laboratories.
Takes place abroad, at laboratories of the group or third parties, not located in Switzerland.
Final cryopreservation
In Switzerland, immediately after processing
In foreign countries, or in Switzerland after bulk reimportation
Temporary initial cryopreservation
Not necessary as at the end of the processing phase the sample is immediately cryopreserved in the same facility.
Abroad
Processing laboratories
Owned by SSCB, located in Switzerland, accredited by FACT–NetCord* and authorized by Swissmedic.
Abroad; no laboratory for production and processing in Switzerland, which takes place abroad, but only facilities for final cryopreservation (temporary cryopreservation in processing countries).
Declared standards
FACT–NetCord, GMP, GDP, Swissmedic compliance (SSCB undergoes periodic inspections)

FACT-NetCord – The global clinical standard specific to cord blood, with stringent requirements for collection, processing, and storage, ensuring inclusion in international transplant registries (and thus the actual usability of the sample in a transplant context) standards_and_accreditation.pdf
Often, generic certifications not specific to cord blood (for example, AABB*) are sometimes not specified in contracts without clarifications regarding the entity to which the standard would have been attributed. GDP (Swissmedic) for export, re-importation to Switzerland

AABB – A more “generic” standard of process and traceability, useful for operational quality, but which does not ensure the same level of clinical acceptance in transplant registries: this means that a unit certified only AABB may not be usable when it is truly needed standards_and_accreditation.pdf
Sample traceability
Total and direct, From the delivery room the biological material arrives without intermediate steps directly to our laboratories where it will be processed and cryopreserved.
Several steps – from the delivery room, the biological material is transported abroad for processing and managed according to the applicable local laws. Only afterwards is it transported in bulk to Switzerland (if applicable).
Transport of biological material (blood, cord tissue, placenta)
Dedicated to each individual customer and within Switzerland: from the delivery room directly to the SSCB laboratories.
Biological material is transported from the delivery room abroad for processing and initial cryopreservation. Only later (if applicable) is it imported in bulk to Switzerland for final storage, with transport terms not always clearly defined in the contracts.
Contractual aspects
Clear contracts: indicate where processing and cryopreservation take place, with reference to standards and laboratories.
Contracts often only mention cryopreservation in Switzerland, without clearly specifying the location of processing, which actually takes place abroad. In some cases, the information is completely omitted, while in others it is expressed in a vague manner, making it difficult to understand exactly where the processing occurs. Processing, according to AABB standards, constitutes a critical and active phase; therefore, one cannot rely solely on the mention of cryopreservation, which instead represents a passive process of simple storage.
Processing of personal data
Exclusive treatment in Switzerland, in accordance with the Federal Act on Data Protection (FADP)
Treatment in Switzerland and abroad
Hybrid banking model
Already available at Inselspital and EOC, only with SSCB upon approval from the Federal Office of Public Health of the Swiss Confederation (UFSP). The goal of the project is to extend it throughout the entire Swiss territory.
Not available
Experience and history
Over 20 years of operation in Switzerland, thousands of families served
Often recent local operators or branches of foreign groups that perform the functions of exporters, reimporters, and storage (without laboratories and permits for processing in Switzerland)
Disposal of excess biological material
Management entirely in Switzerland, processes tracked and verified by Swissmedic
Foreign local regulations and procedures, often not defined in contracts.

The table summarizes some relevant comparison criteria between the standards. It does not claim to be exhaustive or fully applicable to every operator present in Switzerland, but it provides a clear overview of the points that, according to our experience, are of greatest interest to families.