Skip to main content
Autism Stem Care · Istanbul

Clinic Standards & Quality Assurance

Quality, safety, ethics

Quality and safety are not negotiable. Every part of our operation — from cell sourcing to clinical procedures to patient communication — is held to rigorous, documented standards.

Modern GMP clean room with a biosafety cabinet, HEPA ceiling and labelled culture flasks, illustrating the clinical standards and quality assurance behind Autism Stem Care's cell products.
Clinical Care · Istanbul, Türkiye
Certified cell sourcing
GMPCertified cell sourcing
Batches with CoA
100%Batches with CoA
Facility processes
ISO-alignedFacility processes
Ministry-licensed
MoHMinistry-licensed

At Autism Stem Care, the standards behind a treatment matter as much as the treatment itself. We have built our clinical operations to be inspectable, traceable and accountable at every stage.

01Chapter

Cell Product Quality

Our mesenchymal stem cells and exosomes are sourced from GMP-certified (Good Manufacturing Practice) laboratories. Every batch undergoes comprehensive testing.

  • Sterility testing on every batch
  • Cell viability and count verification
  • Potency assessment
  • Genetic stability testing
  • Infectious disease screening
  • Full certificates of analysis available for review and provided on request
Mesenchymal stem cells growing in culture under quality-controlled laboratory conditions
Fig. 01

02Chapter

Clinical Standards

Our clinic operates within accredited medical facilities that meet international standards for patient safety, hygiene, equipment maintenance and emergency preparedness. Treatment protocols follow established clinical guidelines and are designed by our specialised medical team.

03Chapter

Ethical Standards

We adhere to strict ethical principles in every aspect of our practice. We do not make unfounded claims or promise cures. We provide honest, transparent information about benefits and limitations. We obtain informed consent and ensure families understand all aspects of treatment. We maintain patient confidentiality and data protection. We source biological materials ethically, from consenting donors.

Documentation tracing the consented donation and handling of umbilical cord tissue
Fig. 02

04Chapter

Continuous Improvement

We are committed to continuous improvement in our protocols, patient experience and clinical outcomes. We monitor outcomes systematically, stay current with published research, and refine our approaches based on evidence and experience.

Speak with our team

Have questions about whether this is right for your child?

Our medical coordinators reply within 24 hours. No pressure, no commitment — just an honest conversation about your child and what we may (or may not) be able to offer.

From donor to patient

How a single dose is verified

Every cell product follows a documented chain of custody before it ever reaches your child.

  1. Ethical donor sourcing

    Wharton's Jelly tissue from consenting donors with full medical screening.

  2. GMP processing

    Isolation, expansion and characterisation in Good Manufacturing Practice facilities.

  3. Multi-point testing

    Sterility, viability, potency, genetic stability and infectious disease screening.

  4. Certificate of analysis

    A signed certificate of analysis is generated for the specific batch.

  5. Cold-chain logistics

    Transport under temperature-controlled, monitored conditions to the clinic.

  6. Final pre-administration check

    On-site verification immediately before administration to your child.

Verified Credentials

Medical Governance & Accreditation

Republic of Türkiye Ministry of Health
Clinics operate under formal Ministry of Health licensing and inspection — the national regulator for all medical practice in Türkiye.
GMP-Certified Cell Sourcing
MSC and exosome products are sourced from Good Manufacturing Practice laboratories with full batch certificates of analysis.
Turkish Medical Association
Treating physicians are registered members of the Turkish Medical Association (Türk Tabipleri Birliği) and bound by its professional code.
ISO-Aligned Clinical Standards
Facilities follow internationally aligned ISO 9001-style processes for hygiene, equipment maintenance, and emergency preparedness.

Credentials referenced on this page are verified against issuing institutions and re-checked annually as part of our editorial standards.

Clinic Standards — Frequently Asked Questions

GMP — Good Manufacturing Practice — is an internationally recognised quality system that governs how biological products are manufactured, tested and documented to ensure consistency and safety.

Ready to Explore Treatment Options?

Request a free consultation with our medical coordination team. We'll review your child's case and provide personalized guidance.

  • JCI-aligned clinical standards
  • Coordinator response within 24 hours
  • No-obligation medical review

Behind the care

Quality becomes visible in the details

Records, case discussion, traceability, and informed consent turn standards into a process families can see and question.

A technician performing quality-control checks on cell culture vials in a cleanroom
01Traceability at each laboratory checkpoint
The medical team discussing a child's individual treatment plan in a case conference
02Clinical case review across disciplines
A physician reading through a child's diagnostic reports and medical history
03Records reviewed before recommendations

Representative and conceptual imagery. Recommendations depend on individual medical review.