Questions about stem cellsand partnerships, answered

From what mesenchymal stem cells are and where our cells come from, to therapy and institutional partnerships. Type a keyword to filter answers instantly.

About MSCs

Therapy information is for general reference only and is not medical advice. Suitability for any therapy must be decided by a registered physician after assessment.

What are mesenchymal stem cells (MSCs)?

MSCs are a type of stem cell commonly found in the human body. They can self-renew and differentiate into different cell or tissue types such as bone, cartilage and muscle, which is why they matter in tissue repair and regenerative medicine.

Where are MSCs found in the body?

MSCs reside in many organs and tissues, mainly bone marrow, fat tissue and umbilical cord, with smaller amounts elsewhere. Generally, the younger the person, the more stem cells are available.

How does stem cell therapy work?

MSC therapy is a non-surgical, minimally invasive, non-pharmacological approach that aims to support the body’s own repair process. MSCs can differentiate into different cell types and secrete helpful signalling molecules such as cytokines and growth factors, which help regulate inflammation and support the repair of damaged tissue.

In which areas are MSCs being studied?

MSCs are being explored in many clinical studies worldwide, covering the nervous system, bones and joints, cardiovascular health, autoimmunity, and wound and skin repair. Most applications are still at the research stage and do not suit every case; suitability must be judged by a registered physician based on your medical history and test reports.

Sourcing and Quality

Where do Scell Culture Lab stem cells come from?

We work with an award-winning medical laboratory in Canada that is FDA registered, cGMP compliant, and certified to ISO 9001 and ISO 13485 quality management systems. Cells are harvested from donated umbilical cord and bone marrow and cultured there, with very strict donor selection. We also work closely with local Malaysian universities to culture and expand cells in Malaysia.

Why use umbilical cord tissue?

Umbilical cord collection is painless and non-invasive, with no extra extraction needed; supply is relatively plentiful; cord-derived cells are younger and less differentiated, with stronger proliferation; and they have lower immunogenicity, which suits allogeneic use. All donors are screened for infectious diseases to reduce infection risk.

What tests are done before cells are used?

All cells are expanded under safe, stringent procedures. Before use, every batch is tested for viability, contamination (sterility and mycoplasma) and endotoxin, and released only after meeting quality assurance standards.

Do you supply fresh or frozen cells?

We mainly supply fresh live cells, delivered to partners by cold chain with temperature and timing recorded throughout. Every batch comes with a batch test report.

Therapy

Therapy information is for general reference only and is not medical advice. Suitability for any therapy must be decided by a registered physician after assessment.

Who performs the therapy?

Every therapy session is performed by a certified physician.

How are stem cells administered?

Qualified medical personnel administer them by intravenous infusion (drip) or injection; the method is decided by the physician based on the assessment.

Who is suitable for stem cell therapy?

Not everyone is. A medical professional first reviews your medical history and test reports, then advises whether the therapy may help you and which risks to note.

Partnership

Which organisations can become partners?

Licensed hospitals and clinics can discuss fresh live stem cell supply; aesthetic and wellness centres can discuss stem-cell-derived skincare and supplements; businesses, investors and research institutions can discuss cGMP cell lab setup.

What does setting up a cGMP cell lab involve?

We help clients set up and qualify cGMP labs, including licensing registration, routine and complex setups, GMP compliance for existing labs, upgrading and validating existing equipment, and explaining cGMP regulatory requirements for the design, construction and operation of new facilities. Timelines depend on scale and local approvals.

Which regions do you serve?

West Malaysia, East Malaysia, Penang, Singapore, Thailand, Hong Kong and China. Cross-border cooperation must comply with local regulations, which we explain during discussions.

How can I contact you?

WhatsApp +60 12-485 8218 or email [email protected]. A colleague responsible for your area will reply.

Want to explore partnership details?

Ask us on WhatsApp and the colleague responsible will reply.