Mexico-Based Platform
CELLMEX is building its principal laboratory, clinical and administrative platform in Mexico.
CELLMEX works with clinics, hospitals, specialist physicians, research centres and healthcare systems interested in evaluating regenerative medicine programmes, laboratory support, scientific protocols, patient referrals and institutional collaboration.
CELLMEX is developing a regenerative medicine platform intended to support qualified clinics, hospitals and healthcare systems seeking a more structured approach to cellular and cell-free biological technologies.
Institutional collaboration may involve patient referrals, physician consultation, programme development, scientific documentation, laboratory support, professional training or formal research cooperation.
CELLMEX does not assume that one commercial or clinical model is suitable for every institution. The proposed relationship must reflect the facility's medical specialties, licensed professionals, patient population, infrastructure, jurisdiction and intended scope.
Mexico is treated as the primary institutional market. Expansion into the rest of Latin America, including Brazil, requires separate legal, professional, operational and regulatory review.
CELLMEX is building its principal laboratory, clinical and administrative platform in Mexico.
The platform includes MSCs, extracellular vesicles, exosome-related technologies, secretome, conditioned media and advanced cellular research.
Institutional relationships may be developed throughout Latin America on a country-specific basis.
Clinical collaboration may include protocol review, patient eligibility guidance and professional consultation.
CELLMEX approaches regenerative medicine through biological identity, process control, scientific evidence and responsible clinical translation.
Spanish-language regional services are complemented by a separate Portuguese-language strategy for Brazil.
Mexican clinics and hospitals form the primary institutional focus of the CELLMEX development model.
Clinics and hospitals may refer selected patients for medical review and possible treatment at an authorised CELLMEX clinical location.
CELLMEX may discuss the development of a regenerative medicine programme within an appropriately qualified institution.
Institutional enquiries may concern available cellular or cell-free platforms, laboratory capabilities and technical documentation.
Professional education may be developed for approved institutional partners.
CELLMEX may evaluate institutional relationships throughout Latin America, but each country requires its own clinical, legal, regulatory and commercial assessment.
Potential collaboration with specialist physicians, private clinics and hospitals for patient referral, case review and professional education.
Potential institutional, research and physician relationships subject to local requirements and product-specific review.
Potential referral, research and specialist-clinic collaboration following jurisdiction-specific assessment.
Potential academic, hospital and specialist collaborations requiring separate regulatory and operational planning.
Potential referral pathways for eligible patients travelling to Mexico for evaluation or treatment.
Scientific cooperation may include in-vitro, ex-vivo, analytical and translational research.
Brazil should not be treated as a simple extension of the Spanish-speaking Latin American strategy.
Institutional development in Brazil requires Portuguese-language communication, local professional relationships, Brazil-specific regulatory analysis and separate commercial planning.
Potential initial relationships may include research institutions, specialist physicians, private hospitals, biotechnology laboratories and academic medical centres.
Any proposed clinical supply, patient programme, product importation, professional training or research collaboration must be reviewed under the requirements applicable in Brazil.
Structured referral and clinical communication for eligible patients evaluated by CELLMEX.
Development of a defined regenerative medicine service within an appropriately qualified clinic or hospital.
Scientific, technical and clinical education for institutional medical personnel.
Research, analytical, processing or technical cooperation between qualified laboratories.
Joint in-vitro, ex-vivo or translational research under a defined scientific and contractual framework.
Controlled market development involving an institution with suitable clinical, scientific and operational capabilities.
Provide the institution's identity, location, licences, specialties and responsible contacts.
Identify whether the request concerns referrals, protocols, treatment programmes, research or laboratory support.
CELLMEX reviews the medical, scientific, operational and jurisdictional requirements.
Where appropriate, the parties define scope, responsibilities, documentation and next steps.
Collaboration proceeds only after approval of the required legal, professional and operational documentation.
Yes. A referral relationship may be considered after verification of the referring institution and responsible physician.
Patient acceptance remains subject to medical review and does not occur automatically.
Potentially. The proposed programme would require assessment of the institution's physicians, facilities, jurisdiction, clinical capabilities, documentation systems and intended technology.
Product or biological-platform supply should not be assumed. Availability depends on the institution, intended use, jurisdiction, storage capability, professional oversight and applicable requirements.
Yes. Protocol and technical-document requests may be reviewed after professional and institutional verification.
Professional education may be considered for approved partners. Training does not replace medical licensing, specialty competence or institutional credentialing.
Yes. Research proposals should define the scientific objective, methods, biological materials, responsibilities, funding, intellectual property and required approvals.
No. Each country must be reviewed separately. A Mexican agreement or operational model does not automatically authorise clinical use, importation, promotion or distribution in another jurisdiction.
Yes. Brazilian institutions may submit enquiries in Portuguese. Formal implementation should use Portuguese-language clinical, technical and contractual documentation.
Exclusivity should not be assumed. Any territorial, institutional, distribution or representation rights require a separate written agreement and legal review.
CELLMEX will review the institutional profile, objective, responsible professionals, jurisdiction and proposed technology.
If the enquiry is suitable for further review, CELLMEX may request additional documentation or arrange an introductory discussion.
Submission of an enquiry does not establish a partnership, approve a clinical programme, confirm product supply or authorise the use of CELLMEX technologies.
All arrangements remain subject to professional verification, legal documentation, jurisdictional review, internal approval and definition of the parties' respective responsibilities.
Clinical and scientific information must not be converted into unsupported patient advertising or treatment claims.
Complete the form below with sufficient institutional information for an initial review.
Marina Vallarta
Puerto Vallarta, Jalisco
Mexico
Mexico · Latin America · Brazil