Pristine GMP-grade laboratory with microscopes, vials, and soft teal equipment glow, illustrating the clinical standards and quality assurance at Autism Stem Care.

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.

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.

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

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.

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.

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.

Yes. Certificates of analysis for the specific batch used in your child's treatment are available on request, both before and after administration.

Yes. The clinical facilities operate under formal Republic of Türkiye Ministry of Health licensing and inspection.

Medical information is handled with the highest standards of confidentiality, restricted to the clinical team responsible for your child's care.

Any batch that fails any quality benchmark is rejected and never used in patient treatment. A new verified batch is sourced.

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.

Chat with us on WhatsApp