Cell therapy · 2026

Cell therapy in China,
honestly graded.

Stem cells, immune cells (NK · CIK · DC-CIK · CAPRI), exosomes and neonatal cell banking — under one NMPA-regulated framework. China’s first approved MSC drug, four-plus CAR-T approvals, GMP-grade products at Class A hospitals. We grade the evidence honestly and decline cases where cells won’t help.

Jan 2025

First MSC drug approved

Ruibosheng (amimestrocel) — NMPA approval

NMPA, 2025

4+

NMPA-approved CAR-T

Yikaida, Carteyva, Fukerui, Yuanruida

NMPA, 2024

2,794

Registered stem-cell studies

On China Clinical Trial Registry (ChiCTR)

ChiCTR, 2024

4

Cell categories

Stem · immune · exosome · banking

Panda Touring Care

Class A

All partner facilities

NMPA-licensed GMP-grade cellular labs

NHC / NMPA

12 mo

Follow-up included

Telehealth review with operating physician

Panda Touring Care

The case

One framework,
four kinds of cells.

“Cell therapy” covers very different things — regenerative stem cells, cancer-fighting immune cells, cell-free exosomes, and the banking of a newborn’s cells for future use. China regulates all of them through one coherent structure: NMPA-approved cellular drugs plus filed clinical research at Class A hospitals.

That matters because the global cell-therapy market is full of over-promising. After earlier abuses, China deliberately reformed: legitimate treatment now happens only inside the regulated framework. In January 2025 the NMPA approved Ruibosheng — China’s first MSC drug — and four-plus CAR-T products are approved for blood cancers.

For international patients this means real access to evidence-graded protocols at licensed facilities — not ‘cell tourism.’ This hub maps every category and links to the deep dives. Panda Touring Care partners exclusively with NMPA-licensed Class A hospitals including Beijing 301, Shanghai Ruijin, Renji and Boao Lecheng.

How we work

Four principles we won’t bend.

Framework

Two regulated tracks

Cellular drugs approved by NMPA (Ruibosheng MSC, CAR-T), plus filed clinical research (备案) at qualified Class A hospitals. Anything outside this framework is not legitimate — we only use licensed facilities.

E-E-A-T

Honest evidence grading

We grade every indication: strong (GVHD, CAR-T, knee OA), moderate (autoimmune, some oncology adjuncts), emerging (metabolic, neuro). We name what's investigational and decline cases where cell therapy won't help.

Quality

GMP-grade products

Every cellular product is processed in NMPA-licensed GMP labs with release testing — viability, sterility, phenotype (e.g. CD3/CD56 for immune cells), endotoxin and identity verification.

Banking

Whole-family value

Neonatal cell banking stores cord blood, cord tissue, placenta and immune cells once — low immunogenicity means stored samples can serve siblings and parents, not just the child.

We deliberately temper the marketing language common in this field. Broad “anti-ageing” and “cancer-prevention” claims for immune-cell infusions are not supported by high-quality evidence and we will say so. NMPA-approved cellular indications today: GVHD (Ruibosheng) and specific blood cancers (CAR-T). Everything else is delivered as registered clinical research or declined.

The patient pathway

Six steps from inquiry
to 12-month follow-up.

Step 1

Case review

Submit medical records, imaging and current medications. A senior physician determines candidacy, recommends the cell type (stem / immune / exosome) and protocol within 5–7 business days — or tells you honestly if cell therapy isn't indicated.

Step 2

Itemized quote

Receive a written quote covering cell processing, treatment, hospitalization, accommodation and coordinator. Compare 2–3 hospital options where appropriate.

Step 3

M-visa & travel

We issue the hospital invitation letter (3–5 days); M-visa application runs 5–15 business days. Book flexible-date travel.

Step 4

On-site collection / harvest

Consultation, baseline labs and imaging. For autologous cells: harvest from blood, marrow, fat or cord. For allogeneic / banked cells: matching and retrieval. Processing 7–14 days.

Step 5

Infusion & recovery

Cell infusion under medical supervision (IV, intra-articular or intrathecal by indication). On-site recovery with monitoring; discharge when the physician clears.

Step 6

12-month follow-up

Telehealth review at week 2, 6 and months 3, 6, 12 with secure imaging upload. The operating physician remains clinician of record; bilingual records throughout.

FAQ

Cell therapy in China, answered.

What is cell therapy and what types are available in China?
Cell therapy uses living cells — rather than drugs or surgery — to treat, repair or protect the body. China offers four broad categories: (1) Stem cells — mesenchymal stem cells (MSC) for regeneration and immune modulation, now including China's first approved MSC drug, Ruibosheng (amimestrocel, NMPA Jan 2025); (2) Immune cells — NK, CIK, DC-CIK and CAPRI cells used as adjuncts in oncology and immune support, plus NMPA-approved CAR-T for blood cancers; (3) Exosomes — extracellular vesicles secreted by stem cells, used for inflammatory and degenerative conditions; (4) Cell banking — cryopreservation of a newborn's cord blood, cord tissue, placenta and immune cells for future personal or family use.
Is cell therapy legal and regulated in China?
Yes, through two parallel tracks. The drug track: the NMPA approves specific cellular products as drugs — China now has an approved MSC drug (Ruibosheng) and four-plus approved CAR-T products. The clinical-research track: stem-cell and immune-cell treatments are delivered as filed clinical research (备案) at qualified Class A hospitals under National Health Commission and NMPA oversight, following the 2015 regulatory reform. Commercial 'over-the-counter' immune-cell treatment outside this framework is not permitted — a deliberate correction after earlier abuses. International patients should only use NMPA-licensed Class A facilities; Panda Touring Care partners exclusively with these.
What's the difference between stem cells, immune cells and exosomes?
Stem cells (MSC) self-renew and modulate inflammation — used for regeneration, autoimmune and orthopedic conditions. Immune cells (NK / CIK / DC-CIK / CAPRI / CAR-T) are the body's defence cells, expanded and re-infused to recognise and clear abnormal or cancerous cells. Exosomes are nano-sized vesicles released by stem cells that carry their signalling cargo — a cell-free option used for inflammatory and degenerative indications. They are complementary, not interchangeable; your physician recommends based on indication.
Can foreigners receive cell therapy or bank cells in China?
Yes. International patients access NMPA-approved cellular drugs and registered clinical research through dedicated international departments at Class A hospitals with English-speaking coordination. Cell banking (cord blood, cord tissue, placenta) is a commercial storage service available to families. Panda Touring Care manages the full pathway: case review, eligibility assessment, M-visa, on-site treatment or sample collection, and follow-up.
How much does cell therapy cost in China?
All-in pricing including coordinator and on-site stay: autologous MSC $8,400–$24,000; allogeneic MSC $10,000–$28,000; exosome protocols $6,000–$15,000; NK / CIK / DC-CIK immune-cell courses $12,000–$35,000; CAR-T $60,000–$140,000 (vs $400,000+ in the US). Neonatal stem-cell banking is typically $2,000–$6,000 upfront plus ~$150–$400/year storage. Pricing varies by hospital and protocol — request itemized quotes.
Is cell therapy safe and does it actually work?
Honest answer: evidence varies sharply by indication. Strong evidence exists for GVHD (Ruibosheng's approved indication), CAR-T in specific blood cancers, knee osteoarthritis (autologous MSC), and chronic wounds. Immune-cell adjuncts (NK / CIK / DC-CIK) show benefit as add-ons in some oncology trials but are not stand-alone cures; broad anti-ageing and cancer-prevention claims are not supported by high-quality evidence. At NMPA-licensed GMP facilities, serious adverse events in major MSC trials run below 1%. We grade evidence honestly and will tell you when a therapy is investigational.
Where in China should I go for cell therapy?
Top centres: Beijing 301 PLA General Hospital (cellular therapy lab); Beijing PUMC International Department; Shanghai Ruijin Hospital (haematology and stem-cell flagship); Renji Hospital Shanghai (CAR-T leader); Boao Lecheng Pilot Zone in Hainan (special regulatory zone for advanced regenerative therapies); HKU-Shenzhen Hospital (English-first). All operate NMPA-licensed cellular therapy facilities and registered research programmes.

Honest candidacy
assessment, free.

Submit your records and a 30-minute video review with a senior physician will tell you straight which cell therapy — if any — can help, and what realistic outcomes look like for your condition.