Applying cellular biotechnology to clinical practice in Mexico
At Quantum Lab we develop cellular biomaterials under documented quality control and according to national regulatory guidelines.
From research to the clinical setting, driving evidence-based medicine.
At Quantum Lab® we work at the interface between cell biology and medical practice. Our team combines applied research and biotechnological process development to offer cellular materials with traceability, quality control and specialized technical support. We collaborate with healthcare professionals seeking to integrate safe and documented biological tools into their clinical practice.
- 20 years of scientific and clinical experience
- +100 indexed scientific publications
- 80,000 doses applied
- 3,200 lots released
Mission
At Quantum Lab we work to bring cell biology closer to medical practice through standardized, traceable and sustainable processes. Our mission is to provide healthcare professionals with reliable and documented biomaterials that contribute to improving quality of care and patient safety.
Vision
We aspire to consolidate our position as a Latin American reference in applied clinical biotechnology, where research, manufacturing and scientific support converge in the same work model. We seek that each cell preparation we develop maintains the same analytical rigor required in research environments.
Values
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Transparency - access to documentation and quality criteria for each lot.
- Security - release of preparations only after meeting strict standards and documented replenishment protocols.
- Regulatory compliance - operation aligned with NOM, GMP and current guidelines, with evidence available for audit.
- Scientific integrity - validated methods, reference literature and absence of unprovable claims.
- Confidentiality - protection of protocols and clinical data of our collaborators.
What is behind each preparation
We operate culture and analysis laboratories with validated processes and continuous registration.
- We isolate, culture and characterize human cell lines.
- Batch control: identity, viability, microbiology and endotoxins.
- Biosafety areas and reproducible methods.
- Full traceability: receipt → process → release.
- Defined and auditable acceptance criteria.
- Chain of custody and temperature logs.
Sanitary licenses COFEPRIS
Progenitor or Stem Cell Bank No. 253300CT040309
Progenitor or Stem Cell Collection Center No. 253300926A0006
Ethical and institutional support with UNAM
Protocols approved by the Ethics Commission of UNAM (CE/FESI/032024/1710).
Institutional agreement UNAM DGAJ-DPI-070225-1506.