Laboratorio Aclimu
Central Lab & Trials Argentina

Your strategic partner in laboratory services for:Precision Oncology

We operate as Central Lab and Local Lab in Argentina and the region. We process routine, biomarkers, molecular biology and anatomic pathology under ICH-GCP, with a single point of contact per study.

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15+

Years in clinical research

120+

Active studies

30+

Years in operation

Track record

The experience a well-designed study requires.

0+

Years in clinical research

Partnering with local and global sponsors

0+

Active studies

Acting as Central Lab and Local Lab in parallel

0+

Years in operation

Aclimu has been operating since 1994

Capabilities

Routine and specialty, all under one roof.

One chain of custody, one SOP set, one sponsor interface. No need to pass samples through third parties.

PBMC processing + cryopreservation

Isolation of peripheral blood mononuclear cells, viability assessment, aliquoting and storage at -80 °C / LN₂ vapor phase. Traceable cold chain from sample reception.

PBMCCryopreservationViability ≥ 90%LN₂

Routine clinical chemistry

Hematology, clinical chemistry, liver panel, renal function, thyroid panel, hormones and inflammation markers under quality standards.

HematologyChemistryHormones

Specialty biomarkers

Immunoassays, ELISA, flow cytometry, multiplex PCR and HPLC.

ELISAFlow cytometryMultiplex PCRHPLC

Molecular biology and pharmacogenomics

PCR / qPCR, genotyping, gene panels via NGS, MLPA and Array CGH.

NGSqPCRMLPAArray CGH

Anatomic pathology

Histopathology, immunohistochemistry and digital pathology with slide digitization for remote sponsor review.

IHCHistopathDigital pathology

PK/PD bioanalysis

Quantification of drug in plasma and biological matrices. Pharmacokinetic and pharmacodynamic curves with validated methods.

PKPDValidated methods

Sample journey

End-to-end traceability, sample by sample.

    6. 1 / 5

Quality and compliance

Audit-ready any time.

We operate under local and international standards your sponsor or CRO already knows. Each one covers a specific layer: technical, regulatory, data, and transport.

ITAES

Institutional accreditation

Healthcare quality accreditation by the Argentine Institute for Healthcare Establishment Accreditation.

ICH-GCP E6 R3

Good Clinical Practice

We apply the latest (2023) global standard for clinical trial design and conduct.

GLP

Good Laboratory Practice

OECD GLP applied to non-clinical and preclinical studies.

IATA DGR

Biological substances UN3373

Personnel trained in preparation, labeling and international shipping of biological samples.

Law 25.326

Personal data

Compliance with the Argentine privacy law and GDPR considerations for European sponsors.

Trained team

Continuous training

The full team holds the sector's required certifications: GCP, IATA DGR, biosafety, sample handling and any study-specific training required.

Documentation

Online and downloadable

Methods, reference values, current versions and traceability for every determination: available online for sponsors and CROs whenever needed.

ICH-GCP E6 R3·ITAES·Third-party accredited·Chain of custody·Validated methods·End-to-end traceability·Fast turnaround·Trained team·Data confidentiality·Single point of contact·Online documentation·Validated results·ICH-GCP E6 R3·ITAES·Third-party accredited·Chain of custody·Validated methods·End-to-end traceability·Fast turnaround·Trained team·Data confidentiality·Single point of contact·Online documentation·Validated results·

Scientific leadership

Real people, credentials visible.

Every study has a single point of contact and a responsible technical director. No call-center layers between your CRO and the person signing the report.

JG

Technical Director

Dr. Jonatan García

MN 12.541

Responsible for the laboratory's technical direction. Leads method validation processes for multi-site studies and holds all sector certifications required for clinical research.

Areas of expertise

ICH-GCP / ANMAT complianceSponsor and CRO relationsQuality and accreditationBiochemistry

Infrastructure and technology

Validated processes, real-time data.

Study phases

We support Phase I to IV.

Phase I

First-in-human

Small cohorts focused on safety and dosing. We operate as Central Lab with validated methods for PK/PD and safety panels.

PK/PDSafety panelFast turnaround

Phase II

Exploratory efficacy

Biomarkers and efficacy endpoints. Cross-site harmonization and statistical support for interim analyses.

BiomarkersEndpointsInterim analyses

Phase III

Pivotal confirmation

High volume, multi-site. Aclimu integrates into the global trial network or leads the South American region as a local hub.

Regional hubHigh volumeStrict traceability

Phase IV

Post-approval / real-world

Post-market surveillance and effectiveness studies. We process large batches with predictable SLAs.

PharmacovigilanceReal-world dataSLAs

Start a conversation

Every project starts with a good conversation.

We want to understand what you need to solve. We'll respond with a clear proposal — timeline, scope and costs. If we decide to move forward, we'll handle the formal side.

You always speak with the same person from our team.
Custom quote tailored to your study, per module or service.
Smooth integration into your workflow, no downtime.

Direct contact

Single point of contact per study

Write to us

clinicaltrials@aclimu.com.ar

Open under NDA. Share the protocol when signed and we'll respond in detail.